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nsv5501538

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:447

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 113 SVs from 32 studies. See in: genome view    
Submitted genomic52,047,877-52,048,323Question Mark
Overlapping variant regions from other studies: 113 SVs from 32 studies. See in: genome view    
Remapped(Score: Perfect):52,441,661-52,442,107Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5501538Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1252,047,87752,048,323
nsv5501538RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1252,441,66152,442,107

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17058741deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17058741Submitted genomicNC_000012.12:g.520
47877_52048323del
GRCh38 (hg38)NC_000012.12Chr1252,047,87752,048,323
nssv17058741RemappedPerfectNC_000012.11:g.524
41661_52442107del
GRCh37.p13First PassNC_000012.11Chr1252,441,66152,442,107

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)
nssv170587410.01636404
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