A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605535



Internal ID16392944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170085964..170087974hg38UCSC Ensembl
Innerchr6:170401188..170403198hg19UCSC Ensembl
Innerchr6:170243113..170245123hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382011
hg192011
hg182011
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1077399, nssv1077400
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605535
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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