A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv932911



Internal ID16226867
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226284006..226306239hg38UCSC Ensembl
Innerchr2:227148722..227170955hg19UCSC Ensembl
Innerchr2:226856966..226879199hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3822234
hg1922234
hg1822234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584560
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv932911
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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