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nsv5529317

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:1,085

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 150 SVs from 19 studies. See in: genome view    
Submitted genomic29,996,044-29,997,128Question Mark
Overlapping variant regions from other studies: 150 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):30,486,951-30,488,035Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529317Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1929,996,04429,997,128
nsv5529317RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1930,486,95130,488,035

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17722690deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17722690Submitted genomicNC_000019.10:g.299
96044_29997128del
GRCh38 (hg38)NC_000019.10Chr1929,996,04429,997,128
nssv17722690RemappedPerfectNC_000019.9:g.3048
6951_30488035del
GRCh37.p13First PassNC_000019.9Chr1930,486,95130,488,035

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)
nssv17722690<0.00126404
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