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nsv4578072

  • 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: 189 SVs from 6 studies. See in: genome view    
Remapped(Score: Perfect):29,441,614-29,441,614Question Mark
Overlapping variant regions from other studies: 190 SVs from 6 studies. See in: genome view    
Submitted genomic29,459,731-29,459,731Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578072RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX29,441,61429,441,614
nsv4578072Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX29,459,73129,459,731

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16087595alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16087595RemappedPerfectNC_000023.11:g.294
41614_29441615ins2
79
GRCh38.p12First PassNC_000023.11ChrX29,441,61429,441,614
nssv16087595Submitted genomicNC_000023.10:g.294
59731_29459732ins2
79
GRCh37.p13NC_000023.10ChrX29,459,73129,459,731

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)
nssv160875950.0037521630
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