A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv890947



Internal ID15838217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:404077..519032hg38UCSC Ensembl
Innerchr19:404077..519032hg19UCSC Ensembl
Innerchr19:355077..470032hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38114956
hg19114956
hg18114956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578069
Supporting Variants
Samples
Known GenesC2CD4C, MADCAM1, ODF3L2, SHC2, TPGS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv890947
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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