A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899964



Internal ID15847234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46119943..46124941hg38UCSC Ensembl
Innerchr19:46623200..46628198hg19UCSC Ensembl
Innerchr19:51315040..51320038hg18UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg384999
hg194999
hg184999
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579881
Supporting Variants
Samples
Known GenesIGFL3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899964
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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