A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv893182



Internal ID15840452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6677148..6679193hg38UCSC Ensembl
Innerchr19:6677159..6679204hg19UCSC Ensembl
Innerchr19:6628159..6630204hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382046
hg192046
hg182046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578460
Supporting Variants
Samples
Known GenesC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv893182
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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