A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933280



Internal ID16227236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226472641..226482648hg38UCSC Ensembl
Innerchr2:227337357..227347364hg19UCSC Ensembl
Innerchr2:227045601..227055608hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3810008
hg1910008
hg1810008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584596
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)nssv933280
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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