A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv894858



Internal ID15842128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:14621589..14622635hg38UCSC Ensembl
Innerchr19:14732401..14733447hg19UCSC Ensembl
Innerchr19:14593401..14594447hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg381047
hg191047
hg181047
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv578670
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)nssv894858
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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