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nsv5508437

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:109,567

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 349 SVs from 40 studies. See in: genome view    
Submitted genomic75,224,463-75,334,029Question Mark
Overlapping variant regions from other studies: 349 SVs from 40 studies. See in: genome view    
Remapped(Score: Good):74,935,508-75,045,073Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5508437Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000011.10Chr1175,224,46375,334,029
nsv5508437RemappedGoodGRCh37.p13Primary AssemblyFirst PassNC_000011.9Chr1174,935,50875,045,073

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17047202duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17047202Submitted genomicNC_000011.10:g.752
24463_75334029dup
GRCh38 (hg38)NC_000011.10Chr1175,224,46375,334,029
nssv17047202RemappedGoodNC_000011.9:g.7493
5508_75045073dup
GRCh37.p13First PassNC_000011.9Chr1174,935,50875,045,073

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)
nssv17047202<0.00136404
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