A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578612



Internal ID16019335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10271961..10284355hg38UCSC Ensembl
Innerchr19:10382637..10395031hg19UCSC Ensembl
Innerchr19:10243637..10256031hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3812395
hg1912395
hg1812395
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv893546
Samples
Known GenesICAM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578612
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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