A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1051658



Internal ID15558158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:28954942..29374998hg38UCSC Ensembl
Innerchr6:28922719..29342775hg19UCSC Ensembl
Innerchr6:29030698..29450754hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg38420057
hg19420057
hg18420057
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv601213
Supporting Variants
Samples
Known GenesLOC100129636, OR12D3, OR14J1, OR2B3, OR2J2, OR2J3, OR2W1, OR5V1, ZNF311
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1051658
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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