A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515969



Internal ID15096576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:15388939..15406564hg38UCSC Ensembl
InnerchrX:15407061..15424686hg19UCSC Ensembl
InnerchrX:15316982..15334607hg18UCSC Ensembl
InnerchrX:15166718..15184343hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3817626
hg1917626
hg1817626
hg1717626
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv665529, nssv683425, nssv659567
Samples
Known GenesPIR, PIR-FIGF
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515969
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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