A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25789324



Internal ID19159679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43066790..43222743hg38UCSC Ensembl
Innerchr19:43570942..43726895hg19UCSC Ensembl
Innerchr19:48262782..48418735hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38155954
hg19155954
hg18155954
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893217
Supporting Variants
Samples
Known GenesLOC284344, PSG2, PSG4, PSG5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25789324
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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