A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv891796



Internal ID15839066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:1465133..1468329hg38UCSC Ensembl
Innerchr19:1465132..1468328hg19UCSC Ensembl
Innerchr19:1416132..1419328hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg383197
hg193197
hg183197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578287
Supporting Variants
Samples
Known GenesAPC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv891796
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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