A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582049



Internal ID16369458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:56475360..56559965hg38UCSC Ensembl
Innerchr2:56702495..56787100hg19UCSC Ensembl
Innerchr2:56555999..56640604hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3884606
hg1984606
hg1884606
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv911171
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582049
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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