A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604382



Internal ID16391791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:103340397..103384561hg38UCSC Ensembl
Innerchr6:103788272..103832436hg19UCSC Ensembl
Innerchr6:103894965..103939129hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3844165
hg1944165
hg1844165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10884n54
Supporting Variantsnssv1071649
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604382
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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