A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv899525



Internal ID15846795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:41553480..41555570hg38UCSC Ensembl
Innerchr19:42059850..42061940hg19UCSC Ensembl
Innerchr19:46751690..46753780hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382091
hg192091
hg182091
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv579604
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv899525
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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