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nsv4576715

  • 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: 190 SVs from 8 studies. See in: genome view    
Remapped(Score: Perfect):14,004,139-14,004,139Question Mark
Overlapping variant regions from other studies: 191 SVs from 8 studies. See in: genome view    
Submitted genomic14,022,258-14,022,258Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4576715RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX14,004,13914,004,139
nsv4576715Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX14,022,25814,022,258

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16088021alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16088021RemappedPerfectNC_000023.11:g.140
04139_14004140ins2
24
GRCh38.p12First PassNC_000023.11ChrX14,004,13914,004,139
nssv16088021Submitted genomicNC_000023.10:g.140
22258_14022259ins2
24
GRCh37.p13NC_000023.10ChrX14,022,25814,022,258

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)
nssv16088021<0.0011521646
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