A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150667



Internal ID15855121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:3597839..3629432hg38UCSC Ensembl
Innerchr2:3645429..3677022hg19UCSC Ensembl
Innerchr2:3623304..3654897hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3831594
hg1931594
hg1831594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580824
Supporting Variants
Samples1780862444_A
Known GenesCOLEC11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150667
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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