A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608326



Internal ID16049049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:120188277..120355836hg38UCSC Ensembl
Innerchr7:119828331..119995890hg19UCSC Ensembl
Innerchr7:119615567..119783126hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38167560
hg19167560
hg18167560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1093585
Samples
Known GenesKCND2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608326
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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