A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580825



Internal ID16021548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3608153..4065447hg38UCSC Ensembl
Innerchr2:3655743..4113038hg19UCSC Ensembl
Innerchr2:3633618..4090913hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38457295
hg19457296
hg18457296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150668
SamplesHGDP00259
Known GenesALLC, COLEC11, LOC100505964
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580825
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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