A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607237



Internal ID16394646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62524391..63074848hg38UCSC Ensembl
Innerchr7:61984769..62535226hg19UCSC Ensembl
Innerchr7:61622204..62172661hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38550458
hg19550458
hg18550458
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11396n54
Supporting Variantsnssv1085097
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607237
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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