A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605181



Internal ID16045904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162738155..162800760hg38UCSC Ensembl
Innerchr6:163159187..163221792hg19UCSC Ensembl
Innerchr6:163079177..163141782hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3862606
hg1962606
hg1862606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075577
Samples
Known GenesPACRG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605181
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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