A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582765



Internal ID16370174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:117215578..117641566hg38UCSC Ensembl
Innerchr2:117973154..118399142hg19UCSC Ensembl
Innerchr2:117689624..118115612hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg38425989
hg19425989
hg18425989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7020n54
Supporting Variantsnssv916364
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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