A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580822



Internal ID16021545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3552110..4305551hg38UCSC Ensembl
Innerchr2:3599700..4353141hg19UCSC Ensembl
Innerchr2:3577575..4331016hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38753442
hg19753442
hg18753442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903031
Samples
Known GenesALLC, COLEC11, LOC100505964, RNASEH1, RNASEH1-AS1, RPS7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580822
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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