U.S. flag

An official website of the United States government

nsv5428757

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:54,372

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 360 SVs from 29 studies. See in: genome view    
Submitted genomic15,504,398-15,558,769Question Mark
Overlapping variant regions from other studies: 361 SVs from 29 studies. See in: genome view    
Remapped(Score: Perfect):15,522,521-15,576,892Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5428757Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX15,504,39815,558,769
nsv5428757RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX15,522,52115,576,892

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739402duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739402Submitted genomicNC_000023.11:g.155
04398_15558769dup
GRCh38 (hg38)NC_000023.11ChrX15,504,39815,558,769
nssv17739402RemappedPerfectNC_000023.10:g.155
22521_15576892dup
GRCh37.p13First PassNC_000023.10ChrX15,522,52115,576,892

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)
nssv17739402<0.00114805
Support Center