A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605185



Internal ID16392594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162827557..162884394hg38UCSC Ensembl
Innerchr6:163248589..163305426hg19UCSC Ensembl
Innerchr6:163168579..163225416hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3856838
hg1956838
hg1856838
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075581
Samples
Known GenesPACRG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605185
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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