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nsv4578068

  • 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: 175 SVs from 9 studies. See in: genome view    
Remapped(Score: Perfect):46,503,161-46,503,161Question Mark
Overlapping variant regions from other studies: 175 SVs from 9 studies. See in: genome view    
Submitted genomic46,362,596-46,362,596Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578068RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX46,503,16146,503,161
nsv4578068Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX46,362,59646,362,596

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16089611alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16089611RemappedPerfectNC_000023.11:g.465
03161_46503162ins2
81
GRCh38.p12First PassNC_000023.11ChrX46,503,16146,503,161
nssv16089611Submitted genomicNC_000023.10:g.463
62596_46362597ins2
81
GRCh37.p13NC_000023.10ChrX46,362,59646,362,596

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)
nssv160896114.6e-005121648
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