A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607246



Internal ID16394655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62583246..63245808hg38UCSC Ensembl
Innerchr7:62043624..62706186hg19UCSC Ensembl
Innerchr7:61681059..62343621hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38662563
hg19662563
hg18662563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11396n54
Supporting Variantsnssv1085107, nssv1085106
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607246
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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