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nsv4576549

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 184 SVs from 5 studies. See in: genome view    
Remapped(Score: Perfect):129,793,279-129,793,279Question Mark
Overlapping variant regions from other studies: 184 SVs from 5 studies. See in: genome view    
Submitted genomic128,927,255-128,927,255Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4576549RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX129,793,279129,793,279
nsv4576549Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX128,927,255128,927,255

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16090650alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16090650RemappedPerfectNC_000023.11:g.129
793279_129793280in
s281
GRCh38.p12First PassNC_000023.11ChrX129,793,279129,793,279
nssv16090650Submitted genomicNC_000023.10:g.128
927255_128927256in
s281
GRCh37.p13NC_000023.10ChrX128,927,255128,927,255

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)
nssv160906509.2e-005221648
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