A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797017



Internal ID18813898
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:52441917..52732993hg38UCSC Ensembl
Innerchr19:52945170..53236246hg19UCSC Ensembl
Innerchr19:57636982..57928058hg18UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg38291077
hg19291077
hg18291077
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893233
Supporting Variants
Samples
Known GenesZNF137P, ZNF578, ZNF611, ZNF701, ZNF808, ZNF83
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=58
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797017
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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