A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv898777



Internal ID15846047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35268614..35270070hg38UCSC Ensembl
Innerchr19:35759517..35760973hg19UCSC Ensembl
Innerchr19:40451357..40452813hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg381457
hg191457
hg181457
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579395
Supporting Variants
Samples
Known GenesUSF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv898777
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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