U.S. flag

An official website of the United States government

nsv5428656

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:85

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 245 SVs from 23 studies. See in: genome view    
Submitted genomic54,998,917-54,999,001Question Mark
Overlapping variant regions from other studies: 239 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):55,025,350-55,025,434Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5428656Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX54,998,91754,999,001
nsv5428656RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX55,025,35055,025,434

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740183deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740183Submitted genomicNC_000023.11:g.549
98917_54999001del
GRCh38 (hg38)NC_000023.11ChrX54,998,91754,999,001
nssv17740183RemappedPerfectNC_000023.10:g.550
25350_55025434del
GRCh37.p13First PassNC_000023.10ChrX55,025,35055,025,434

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)
nssv17740183<0.00116404
Support Center