A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv613252



Internal ID16053975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6715730..7022554hg38UCSC Ensembl
Innerchr9:6715730..7022554hg19UCSC Ensembl
Innerchr9:6705730..7012554hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38306825
hg19306825
hg18306825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1126840
Samples
Known GenesKDM4C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv613252
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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