A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899935



Internal ID15847205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:45334025..45359625hg38UCSC Ensembl
Innerchr19:45837283..45862883hg19UCSC Ensembl
Innerchr19:50529123..50554723hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3825601
hg1925601
hg1825601
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579868
Supporting Variants
Samples
Known GenesERCC2, KLC3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899935
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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