A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893169



Internal ID18837303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19838400..19973913hg38UCSC Ensembl
Outerchr19:19838400..19973913hg38UCSC Ensembl
Innerchr19:19949209..20084722hg19UCSC Ensembl
Outerchr19:19949209..20084722hg19UCSC Ensembl
Innerchr19:19810209..19945722hg18UCSC Ensembl
Outerchr19:19810209..19945722hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38135514
hg19135514
hg18135514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782127
Samples
Known GenesZNF253, ZNF93
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893169
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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