A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv578456



Internal ID16365865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5504701..5510656hg38UCSC Ensembl
Innerchr19:5504712..5510667hg19UCSC Ensembl
Innerchr19:5455712..5461667hg18UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385956
hg195956
hg185956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv892938
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv578456
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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