A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582781



Internal ID16370190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:118432725..118534538hg38UCSC Ensembl
Innerchr2:119190301..119292114hg19UCSC Ensembl
Innerchr2:118906771..119008584hg18UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38101814
hg19101814
hg18101814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv916426
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582781
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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