A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152218



Internal ID15526777
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21733..143598hg38UCSC Ensembl
Innerchr3:63411..185281hg19UCSC Ensembl
Innerchr3:38411..160281hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38121866
hg19121871
hg18121871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589234
Supporting Variants
SamplesHGDP00208
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152218
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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