A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607663



Internal ID16395072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79352403..79401606hg38UCSC Ensembl
Innerchr7:78981719..79030922hg19UCSC Ensembl
Innerchr7:78819655..78868858hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3849204
hg1949204
hg1849204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1155210
Samples1782681316_A
Known GenesMAGI2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607663
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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