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nsv5405370

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 146 SVs from 27 studies. See in: genome view    
Submitted genomic108,815,362-108,815,413Question Mark
Overlapping variant regions from other studies: 147 SVs from 27 studies. See in: genome view    
Remapped(Score: Perfect):109,357,984-109,358,035Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5405370Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1108,815,362108,815,413
nsv5405370RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1109,357,984109,358,035

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16907988alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16907988Submitted genomicNC_000001.11:g.108
815362_108815413in
s281
GRCh38 (hg38)NC_000001.11Chr1108,815,362108,815,413
nssv16907988RemappedPerfectNC_000001.10:g.109
357984_109358035in
s281
GRCh37.p13First PassNC_000001.10Chr1109,357,984109,358,035

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)
nssv16907988<0.00126404
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