A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521297



Internal ID15101904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:114144971..114555695hg38UCSC Ensembl
InnerchrX:113388185..113790147hg19UCSC Ensembl
InnerchrX:113274437..113696403hg18UCSC Ensembl
InnerchrX:113193926..113613127hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38410725
hg19401963
hg18421967
hg17419202
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv524n21
Supporting Variantsnssv697903
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521297
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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