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nsv5495948

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,898

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 162 SVs from 44 studies. See in: genome view    
Submitted genomic63,842,317-63,875,214Question Mark
Overlapping variant regions from other studies: 162 SVs from 44 studies. See in: genome view    
Remapped(Score: Perfect):63,609,789-63,642,686Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5495948Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1163,842,31763,875,214
nsv5495948RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1163,609,78963,642,686

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17046663deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17046663Submitted genomicNC_000011.10:g.638
42317_63875214del
GRCh38 (hg38)NC_000011.10Chr1163,842,31763,875,214
nssv17046663RemappedPerfectNC_000011.9:g.6360
9789_63642686del
GRCh37.p13First PassNC_000011.9Chr1163,609,78963,642,686

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)
nssv17046663<0.00126404
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