A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782127



Internal ID18816411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19838400..19973913hg38UCSC Ensembl
Innerchr19:19949209..20084722hg19UCSC Ensembl
Innerchr19:19810209..19945722hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38135514
hg19135514
hg18135514
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893169
Supporting Variants
Samples
Known GenesZNF253, ZNF93
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=14
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782127
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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