A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580836



Internal ID16368245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3916275..4782952hg38UCSC Ensembl
Innerchr2:3963865..4830542hg19UCSC Ensembl
Innerchr2:3941740..4808417hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38866678
hg19866678
hg18866678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903065
Samples
Known GenesLOC100505964, LOC727982
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580836
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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