A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606358



Internal ID16047081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18045220..18376474hg38UCSC Ensembl
Innerchr7:18084843..18416097hg19UCSC Ensembl
Innerchr7:18051368..18382622hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38331255
hg19331255
hg18331255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079648
Samples
Known GenesHDAC9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606358
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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