A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3564792



Internal ID18516387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:15197257..15238422hg38UCSC Ensembl
Innerchr19:15308068..15349233hg19UCSC Ensembl
Innerchr19:15169068..15210233hg18UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3841166
hg1941166
hg1841166
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060266
Supporting Variants
Samples
Known GenesBRD4, EPHX3, NOTCH3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3564792
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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