A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155783



Internal ID15526686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:134914396..135161428hg38UCSC Ensembl
Innerchr6:135235534..135482566hg19UCSC Ensembl
Innerchr6:135277227..135524259hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg38247033
hg19247033
hg18247033
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604723
Supporting Variants
SamplesHGDP00181
Known GenesALDH8A1, HBS1L, MIR3662
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155783
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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