A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526427



Internal ID15453720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113565754..113698901hg38UCSC Ensembl
InnerchrX:112809041..112942188hg19UCSC Ensembl
InnerchrX:112695700..112828515hg18UCSC Ensembl
InnerchrX:112615189..112748004hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38133148
hg19133148
hg18132816
hg17132816
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702729
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526427
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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