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nsv5414344

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:2,135

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 248 SVs from 21 studies. See in: genome view    
Submitted genomic134,386,900-134,389,034Question Mark
Overlapping variant regions from other studies: 248 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):133,520,930-133,523,064Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5414344Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX134,386,900134,389,034
nsv5414344RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX133,520,930133,523,064

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17742432deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17742432Submitted genomicNC_000023.11:g.134
386900_134389034de
l
GRCh38 (hg38)NC_000023.11ChrX134,386,900134,389,034
nssv17742432RemappedPerfectNC_000023.10:g.133
520930_133523064de
l
GRCh37.p13First PassNC_000023.10ChrX133,520,930133,523,064

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)
nssv17742432<0.00136404
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