A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792590



Internal ID18824236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22163601..23022762hg38UCSC Ensembl
Innerchr19:22346403..23205564hg19UCSC Ensembl
Innerchr19:22138243..22997404hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38859162
hg19859162
hg18859162
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893182
Supporting Variants
Samples
Known GenesLOC100996349, LOC440518, ZNF492, ZNF676, ZNF728, ZNF729, ZNF98, ZNF99
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=179
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792590
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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