A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527438



Internal ID15108045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:76610412..76615326hg38UCSC Ensembl
Innerchr9:79225328..79230242hg19UCSC Ensembl
Innerchr9:78415148..78420062hg18UCSC Ensembl
Innerchr9:76454882..76459796hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg384915
hg194915
hg184915
hg174915
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703878
Samples
Known GenesPRUNE2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527438
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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