A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606279



Internal ID16047002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13955584..13988366hg38UCSC Ensembl
Innerchr7:13995209..14027991hg19UCSC Ensembl
Innerchr7:13961734..13994516hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3832783
hg1932783
hg1832783
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1079282
Samples
Known GenesETV1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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