A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580771



Internal ID16368180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:2897989..2936349hg38UCSC Ensembl
Innerchr2:2901761..2940121hg19UCSC Ensembl
Innerchr2:2880768..2919128hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3838361
hg1938361
hg1838361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv902730
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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