A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584814



Internal ID16372223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:240624322..240648033hg38UCSC Ensembl
Innerchr2:241563739..241587450hg19UCSC Ensembl
Innerchr2:241212412..241236123hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3823712
hg1923712
hg1823712
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv933830
Samples
Known GenesGPR35
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584814
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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