A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899938



Internal ID16193894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46102289..46111139hg38UCSC Ensembl
Innerchr19:46605547..46614397hg19UCSC Ensembl
Innerchr19:51297387..51306237hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg388851
hg198851
hg188851
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579871
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899938
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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