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nsv4578207

  • 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: 183 SVs from 7 studies. See in: genome view    
Remapped(Score: Perfect):124,421,364-124,421,364Question Mark
Overlapping variant regions from other studies: 183 SVs from 7 studies. See in: genome view    
Submitted genomic123,555,214-123,555,214Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4578207RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX124,421,364124,421,364
nsv4578207Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX123,555,214123,555,214

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16089125alu insertionSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16089125RemappedPerfectNC_000023.11:g.124
421364_124421365in
s280
GRCh38.p12First PassNC_000023.11ChrX124,421,364124,421,364
nssv16089125Submitted genomicNC_000023.10:g.123
555214_123555215in
s280
GRCh37.p13NC_000023.10ChrX123,555,214123,555,214

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)
nssv160891254.6e-005121648
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