A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788864



Internal ID18821233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:22155340..23022762hg38UCSC Ensembl
Innerchr19:22338142..23205564hg19UCSC Ensembl
Innerchr19:22129982..22997404hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38867423
hg19867423
hg18867423
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=180
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788864
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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