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nsv5431269

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,538

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 291 SVs from 36 studies. See in: genome view    
Submitted genomic110,695,374-110,698,911Question Mark
Overlapping variant regions from other studies: 291 SVs from 36 studies. See in: genome view    
Remapped(Score: Perfect):109,938,602-109,942,139Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5431269Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX110,695,374110,698,911
nsv5431269RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX109,938,602109,942,139

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741965deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741965Submitted genomicNC_000023.11:g.110
695374_110698911de
l
GRCh38 (hg38)NC_000023.11ChrX110,695,374110,698,911
nssv17741965RemappedPerfectNC_000023.10:g.109
938602_109942139de
l
GRCh37.p13First PassNC_000023.10ChrX109,938,602109,942,139

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)
nssv177419650.006376404
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