A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933633



Internal ID15880903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:232463920..232508140hg38UCSC Ensembl
Innerchr2:233328630..233372850hg19UCSC Ensembl
Innerchr2:233036874..233081094hg18UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3844221
hg1944221
hg1844221
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584694
Supporting Variants
Samples
Known GenesECEL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933633
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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