A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893201



Internal ID18837335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:36973473..37170023hg38UCSC Ensembl
Outerchr19:36973473..37170023hg38UCSC Ensembl
Innerchr19:37464375..37660925hg19UCSC Ensembl
Outerchr19:37464375..37660925hg19UCSC Ensembl
Innerchr19:42156215..42352765hg18UCSC Ensembl
Outerchr19:42156215..42352765hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38196551
hg19196551
hg18196551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791344
Samples
Known GenesZNF420, ZNF568, ZNF585A
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893201
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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