A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582477



Internal ID16369886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:92021069..92120369hg38UCSC Ensembl
Innerchr2:92209095..92308395hg19UCSC Ensembl
Innerchr2:91572822..91672122hg18UCSC Ensembl
Cytoband2p11.1
Allele length
AssemblyAllele length
hg3899301
hg1999301
hg1899301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv914064
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582477
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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