A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv894576



Internal ID16188532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:13665213..13678835hg38UCSC Ensembl
Innerchr19:13776027..13789649hg19UCSC Ensembl
Innerchr19:13637027..13650649hg18UCSC Ensembl
Cytoband19p13.13
Allele length
AssemblyAllele length
hg3813623
hg1913623
hg1813623
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578638
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)nssv894576
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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