A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609001



Internal ID16049724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150909200..150970122hg38UCSC Ensembl
Innerchr7:150606288..150667210hg19UCSC Ensembl
Innerchr7:150237221..150298143hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3860923
hg1960923
hg1860923
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11721n54
Supporting Variantsnssv1155700
SamplesHGDP01027
Known GenesKCNH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609001
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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