A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582732



Internal ID16370141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:115043032..115077076hg38UCSC Ensembl
Innerchr2:115800609..115834653hg19UCSC Ensembl
Innerchr2:115517079..115551123hg18UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg3834045
hg1934045
hg1834045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv916285, nssv1150491, nssv1150492
Samples1780862459_A, 1780862001_A
Known GenesDPP10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582732
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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