U.S. flag

An official website of the United States government

nsv5555883

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 247 SVs from 20 studies. See in: genome view    
Submitted genomic111,894,029-111,894,080Question Mark
Overlapping variant regions from other studies: 247 SVs from 20 studies. See in: genome view    
Remapped(Score: Perfect):111,137,257-111,137,308Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5555883Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX111,894,029111,894,080
nsv5555883RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX111,137,257111,137,308

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17741994alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17741994Submitted genomicNC_000023.11:g.111
894029_111894080in
s195
GRCh38 (hg38)NC_000023.11ChrX111,894,029111,894,080
nssv17741994RemappedPerfectNC_000023.10:g.111
137257_111137308in
s195
GRCh37.p13First PassNC_000023.10ChrX111,137,257111,137,308

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)
nssv17741994<0.00126404
Support Center