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nsv6138208

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:170,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 549 SVs from 57 studies. See in: genome view    
Submitted genomic123,503,381-123,673,381Question Mark
Overlapping variant regions from other studies: 549 SVs from 57 studies. See in: genome view    
Remapped(Score: Perfect):122,637,232-122,807,232Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv6138208Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX123,503,381123,673,381
nsv6138208RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX122,637,232122,807,232

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17737481duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17737481Submitted genomicNC_000023.11:g.123
503381_123673381du
p
GRCh38 (hg38)NC_000023.11ChrX123,503,381123,673,381
nssv17737481RemappedPerfectNC_000023.10:g.122
637232_122807232du
p
GRCh37.p13First PassNC_000023.10ChrX122,637,232122,807,232

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)
nssv17737481<0.00134781
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