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nsv5527065

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:27,471

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 248 SVs from 46 studies. See in: genome view    
Submitted genomic47,700,531-47,728,001Question Mark
Overlapping variant regions from other studies: 248 SVs from 46 studies. See in: genome view    
Remapped(Score: Perfect):48,203,788-48,231,258Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5527065Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1947,700,53147,728,001
nsv5527065RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1948,203,78848,231,258

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723793duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723793Submitted genomicNC_000019.10:g.477
00531_47728001dup
GRCh38 (hg38)NC_000019.10Chr1947,700,53147,728,001
nssv17723793RemappedPerfectNC_000019.9:g.4820
3788_48231258dup
GRCh37.p13First PassNC_000019.9Chr1948,203,78848,231,258

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)
nssv17723793<0.00126404
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