A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601216



Internal ID16041939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29016735..29224369hg38UCSC Ensembl
Innerchr6:28984512..29192146hg19UCSC Ensembl
Innerchr6:29092491..29300125hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38207635
hg19207635
hg18207635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1051661
Samples
Known GenesLOC100129636, OR2B3, OR2J2, OR2J3, OR2W1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601216
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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