A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582771



Internal ID16370180
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:118123425..118124611hg38UCSC Ensembl
Innerchr2:118881001..118882187hg19UCSC Ensembl
Innerchr2:118597471..118598657hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381187
hg191187
hg181187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7022n54
Supporting Variantsnssv916369
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582771
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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