A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893168



Internal ID18837302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19760441..19779641hg38UCSC Ensembl
Outerchr19:19760441..19797524hg38UCSC Ensembl
Innerchr19:19871250..19890450hg19UCSC Ensembl
Outerchr19:19871250..19908333hg19UCSC Ensembl
Innerchr19:19732250..19751450hg18UCSC Ensembl
Outerchr19:19732250..19769333hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3837084
hg1937084
hg1837084
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782126, essv25792737
Samples
Known GenesLINC00663, ZNF506
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893168
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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