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nsv5427133

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:20,696

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 309 SVs from 41 studies. See in: genome view    
Submitted genomic130,377,232-130,397,927Question Mark
Overlapping variant regions from other studies: 309 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):129,511,206-129,531,901Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5427133Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX130,377,232130,397,927
nsv5427133RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX129,511,206129,531,901

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17737572duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17737572Submitted genomicNC_000023.11:g.130
377232_130397927du
p
GRCh38 (hg38)NC_000023.11ChrX130,377,232130,397,927
nssv17737572RemappedPerfectNC_000023.10:g.129
511206_129531901du
p
GRCh37.p13First PassNC_000023.10ChrX129,511,206129,531,901

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)
nssv177375720.00294804
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