A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv892069



Internal ID15839339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2120155..2129040hg38UCSC Ensembl
Innerchr19:2120154..2129039hg19UCSC Ensembl
Innerchr19:2071154..2080039hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388886
hg198886
hg188886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578381
Supporting Variants
Samples
Known GenesAP3D1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv892069
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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