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nsv4034377

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:519,829

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 542 SVs from 19 studies. See in: genome view    
Remapped(Score: Perfect):4,593,415-5,113,243Question Mark
Overlapping variant regions from other studies: 543 SVs from 19 studies. See in: genome view    
Submitted genomic4,511,456-5,031,284Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4034377RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000023.11ChrX4,593,4155,113,243
nsv4034377Submitted genomicGRCh37.p13Primary AssemblyNC_000023.10ChrX4,511,4565,031,284

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv15987767duplicationSequencingOther

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv15987767RemappedPerfectNC_000023.11:g.459
3415_5113243dup
GRCh38.p12First PassNC_000023.11ChrX4,593,4155,113,243
nssv15987767Submitted genomicNC_000023.10:g.451
1456_5031284dup
GRCh37.p13NC_000023.10ChrX4,511,4565,031,284

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)
nssv15987767<0.001421036
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