A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604462



Internal ID16391871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:108289636..108292170hg38UCSC Ensembl
Innerchr6:108610840..108613374hg19UCSC Ensembl
Innerchr6:108717533..108720067hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382535
hg192535
hg182535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10900n54
Supporting Variantsnssv1071932
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604462
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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