A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933279



Internal ID16227235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:226472641..226481238hg38UCSC Ensembl
Innerchr2:227337357..227345954hg19UCSC Ensembl
Innerchr2:227045601..227054198hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg388598
hg198598
hg188598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584595
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)nssv933279
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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