A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606620



Internal ID16394029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:36691170..36736167hg38UCSC Ensembl
Innerchr7:36730775..36775772hg19UCSC Ensembl
Innerchr7:36697300..36742297hg18UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3844998
hg1944998
hg1844998
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155167
SamplesHGDP00866
Known GenesAOAH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606620
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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