A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606224



Internal ID16046947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:12367200..12496710hg38UCSC Ensembl
Innerchr7:12406826..12536336hg19UCSC Ensembl
Innerchr7:12373351..12502861hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38129511
hg19129511
hg18129511
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079182
Samples
Known GenesVWDE
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606224
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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