A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521498



Internal ID15102105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113498514..113673809hg38UCSC Ensembl
InnerchrX:112741785..112917096hg19UCSC Ensembl
InnerchrX:112628441..112803423hg18UCSC Ensembl
InnerchrX:112547930..112722912hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38175296
hg19175312
hg18174983
hg17174983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698112
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521498
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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