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nsv5559869

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 310 SVs from 21 studies. See in: genome view    
Submitted genomic13,745,893-13,745,944Question Mark
Overlapping variant regions from other studies: 311 SVs from 21 studies. See in: genome view    
Remapped(Score: Perfect):13,764,012-13,764,063Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5559869Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000023.11ChrX13,745,89313,745,944
nsv5559869RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000023.10ChrX13,764,01213,764,063

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17739331alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17739331Submitted genomicNC_000023.11:g.137
45893_13745944ins2
61
GRCh38 (hg38)NC_000023.11ChrX13,745,89313,745,944
nssv17739331RemappedPerfectNC_000023.10:g.137
64012_13764063ins2
61
GRCh37.p13First PassNC_000023.10ChrX13,764,01213,764,063

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)
nssv17739331<0.00126404
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