A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583291



Internal ID16370700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:149122777..149135892hg38UCSC Ensembl
Innerchr2:149979291..149992406hg19UCSC Ensembl
Innerchr2:149687537..149700652hg18UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg3813116
hg1913116
hg1813116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150786
Samples1798860565_A
Known GenesLYPD6B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583291
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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