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nsv6138391

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:348,513

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1141 SVs from 60 studies. See in: genome view    
Submitted genomic4,597,488-4,946,000Question Mark
Overlapping variant regions from other studies: 1142 SVs from 60 studies. See in: genome view    
Remapped(Score: Perfect):4,515,529-4,864,041Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6138391Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX4,597,4884,946,000
nsv6138391RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX4,515,5294,864,041

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17736161duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17736161Submitted genomicNC_000023.11:g.459
7488_4946000dup
GRCh38 (hg38)NC_000023.11ChrX4,597,4884,946,000
nssv17736161RemappedPerfectNC_000023.10:g.451
5529_4864041dup
GRCh37.p13First PassNC_000023.10ChrX4,515,5294,864,041

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)
nssv17736161<0.00134783
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