A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578076



Internal ID16018799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:404128..423625hg38UCSC Ensembl
Innerchr19:404128..423625hg19UCSC Ensembl
Innerchr19:355128..374625hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3819498
hg1919498
hg1819498
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6153n54
Supporting Variantsnssv890970
Samples
Known GenesC2CD4C, SHC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578076
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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