A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893233



Internal ID18837367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52441917..52732993hg38UCSC Ensembl
Outerchr19:52438287..52733078hg38UCSC Ensembl
Innerchr19:52945170..53236246hg19UCSC Ensembl
Outerchr19:52941540..53236331hg19UCSC Ensembl
Innerchr19:57636982..57928058hg18UCSC Ensembl
Outerchr19:57633352..57928143hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38294792
hg19294792
hg18294792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25800346, essv25797017
Samples
Known GenesZNF137P, ZNF534, ZNF578, ZNF611, ZNF701, ZNF808, ZNF83
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893233
Frequency
Sample Size3017
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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