A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580985



Internal ID16368394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:11879024..11887185hg38UCSC Ensembl
Innerchr2:12019150..12027311hg19UCSC Ensembl
Innerchr2:11936601..11944762hg18UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg388162
hg198162
hg188162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv903762
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580985
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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