A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789754



Internal ID18835861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:58088681..58218467hg38UCSC Ensembl
Innerchr19:58600048..58729833hg19UCSC Ensembl
Innerchr19:63291860..63421645hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg38129787
hg19129786
hg18129786
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893260
Supporting Variants
Samples
Known GenesZNF274, ZNF329, ZSCAN18
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=28
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789754
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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