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nsv6138507

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:447,101

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 790 SVs from 48 studies. See in: genome view    
Submitted genomic55,728,000-56,175,100Question Mark
Overlapping variant regions from other studies: 789 SVs from 48 studies. See in: genome view    
Remapped(Score: Perfect):55,754,433-56,201,533Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6138507Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX55,728,00056,175,100
nsv6138507RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX55,754,43356,201,533

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17740215duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17740215Submitted genomicNC_000023.11:g.557
28000_56175100dup
GRCh38 (hg38)NC_000023.11ChrX55,728,00056,175,100
nssv17740215RemappedPerfectNC_000023.10:g.557
54433_56201533dup
GRCh37.p13First PassNC_000023.10ChrX55,754,43356,201,533

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)
nssv17740215<0.00134779
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