A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606347



Internal ID16393756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:17360234..17589927hg38UCSC Ensembl
Innerchr7:17399858..17629551hg19UCSC Ensembl
Innerchr7:17366383..17596076hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg38229694
hg19229694
hg18229694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11226n54
Supporting Variantsnssv1155308
Samples1782681286_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606347
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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