A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578502



Internal ID16365911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:7112582..7205229hg38UCSC Ensembl
Innerchr19:7112593..7205240hg19UCSC Ensembl
Innerchr19:7063593..7156240hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3892648
hg1992648
hg1892648
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150034
SamplesHGDP01102
Known GenesINSR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578502
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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