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nsv4625763

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 354 SVs from 65 studies. See in: genome view    
    Remapped(Score: Perfect):54,220,709-54,220,762Question Mark
    Overlapping variant regions from other studies: 262 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):195,693-195,746Question Mark
    Overlapping variant regions from other studies: 256 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):195,697-195,750Question Mark
    Overlapping variant regions from other studies: 260 SVs from 52 studies. See in: genome view    
    Remapped(Score: Perfect):195,509-195,562Question Mark
    Overlapping variant regions from other studies: 312 SVs from 56 studies. See in: genome view    
    Submitted genomic54,724,579-54,724,632Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
    nsv4625763RemappedPerfectGRCh38.p12Primary AssemblySecond PassNC_000019.10Chr1954,220,70954,220,762
    nsv4625763RemappedPerfectGRCh38.p12ALT_REF_LOCI_9First PassNT_187693.1Chr19|NT_1
    87693.1    		195,693195,746
    nsv4625763RemappedPerfectGRCh38.p12ALT_REF_LOCI_7Second PassNW_003571060.1Chr19|NW_0
    03571060.1    		195,697195,750
    nsv4625763RemappedPerfectGRCh38.p12ALT_REF_LOCI_1Second PassNW_003571054.1Chr19|NW_0
    03571054.1    		195,509195,562
    nsv4625763Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000019.9Chr1954,724,57954,724,632

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv16135634deletionCuratedCurated
    nssv16139905duplicationCuratedCurated

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
    nssv16135634RemappedPerfectNT_187693.1:g.(?_1
    95693)_(195746_?)d
    el    		GRCh38.p12First PassNT_187693.1Chr19|NT_1
    87693.1    		195,693195,746
    nssv16139905RemappedPerfectNT_187693.1:g.(?_1
    95693)_(195746_?)d
    up    		GRCh38.p12First PassNT_187693.1Chr19|NT_1
    87693.1    		195,693195,746
    nssv16135634RemappedPerfectNW_003571060.1:g.(
    ?_195697)_(195750_
    ?)del    		GRCh38.p12Second PassNW_003571060.1Chr19|NW_0
    03571060.1    		195,697195,750
    nssv16139905RemappedPerfectNW_003571060.1:g.(
    ?_195697)_(195750_
    ?)dup    		GRCh38.p12Second PassNW_003571060.1Chr19|NW_0
    03571060.1    		195,697195,750
    nssv16135634RemappedPerfectNW_003571054.1:g.(
    ?_195509)_(195562_
    ?)del    		GRCh38.p12Second PassNW_003571054.1Chr19|NW_0
    03571054.1    		195,509195,562
    nssv16139905RemappedPerfectNW_003571054.1:g.(
    ?_195509)_(195562_
    ?)dup    		GRCh38.p12Second PassNW_003571054.1Chr19|NW_0
    03571054.1    		195,509195,562
    nssv16135634RemappedPerfectNC_000019.10:g.(?_
    54220709)_(5422076
    2_?)del    		GRCh38.p12Second PassNC_000019.10Chr1954,220,70954,220,762
    nssv16139905RemappedPerfectNC_000019.10:g.(?_
    54220709)_(5422076
    2_?)dup    		GRCh38.p12Second PassNC_000019.10Chr1954,220,70954,220,762
    nssv16135634Submitted genomicNC_000019.9:g.(?_5
    4724579)_(54724632
    _?)del    		GRCh37 (hg19)NC_000019.9Chr1954,724,57954,724,632
    nssv16139905Submitted genomicNC_000019.9:g.(?_5
    4724579)_(54724632
    _?)dup    		GRCh37 (hg19)NC_000019.9Chr1954,724,57954,724,632

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv161356340.08572845
    nssv161399050.01714845
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