A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv919660



Internal ID15866930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:127043405..127110859hg38UCSC Ensembl
Innerchr2:127800981..127868435hg19UCSC Ensembl
Innerchr2:127517451..127584905hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3867455
hg1967455
hg1867455
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583033
Supporting Variants
Samples
Known GenesBIN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv919660
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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