A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv894859



Internal ID15842129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14621589..14622711hg38UCSC Ensembl
Innerchr19:14732401..14733523hg19UCSC Ensembl
Innerchr19:14593401..14594523hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381123
hg191123
hg181123
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578671
Supporting Variants
Samples
Known GenesEMR3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv894859
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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