U.S. flag

An official website of the United States government

nsv5430803

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:56

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 244 SVs from 19 studies. See in: genome view    
Submitted genomic134,490,459-134,490,514Question Mark
Overlapping variant regions from other studies: 244 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):133,624,489-133,624,544Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5430803Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX134,490,459134,490,514
nsv5430803RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX133,624,489133,624,544

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17742435deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17742435Submitted genomicNC_000023.11:g.134
490459_134490514de
l
GRCh38 (hg38)NC_000023.11ChrX134,490,459134,490,514
nssv17742435RemappedPerfectNC_000023.10:g.133
624489_133624544de
l
GRCh37.p13First PassNC_000023.10ChrX133,624,489133,624,544

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)
nssv17742435<0.00116404
Support Center