A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566522



Internal ID18864803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:28001896..28215779hg38UCSC Ensembl
Innerchr19:28492803..28706686hg19UCSC Ensembl
Innerchr19:33184643..33398526hg18UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg38213884
hg19213884
hg18213884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062160
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566522
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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