A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150491



Internal ID15854162
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 StatusS
Merged Variantsnsv582732
Supporting Variants
Samples1780862001_A
Known GenesDPP10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150491
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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