A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602760



Internal ID16390169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32644878..32658309hg38UCSC Ensembl
Innerchr6:32612655..32626086hg19UCSC Ensembl
Innerchr6:32720633..32734064hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3813432
hg1913432
hg1813432
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10595n54
Supporting Variantsnssv1056782
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602760
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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