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nsv4536962

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:200,302

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 227 SVs from 15 studies. See in: genome view    
Remapped(Score: Perfect):35,819,097-36,019,398Question Mark
Overlapping variant regions from other studies: 227 SVs from 15 studies. See in: genome view    
Submitted genomic36,309,999-36,510,300Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4536962RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000019.10Chr1935,819,09736,019,398
nsv4536962Submitted genomicGRCh37.p13Primary AssemblyNC_000019.9Chr1936,309,99936,510,300

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15961609duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15961609RemappedPerfectNC_000019.10:g.358
19097_36019398dup
GRCh38.p12First PassNC_000019.10Chr1935,819,09736,019,398
nssv15961609Submitted genomicNC_000019.9:g.3630
9999_36510300dup
GRCh37.p13NC_000019.9Chr1936,309,99936,510,300

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv159616094.6e-005121694
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