A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893187



Internal ID19184007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:23755600..24058822hg38UCSC Ensembl
Outerchr19:23755600..24058822hg38UCSC Ensembl
Innerchr19:23938402..24241624hg19UCSC Ensembl
Outerchr19:23938402..24241624hg19UCSC Ensembl
Innerchr19:23730242..24033464hg18UCSC Ensembl
Outerchr19:23730242..24033464hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38303223
hg19303223
hg18303223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789158
Samples
Known GenesRPSAP58, ZNF254, ZNF681, ZNF726
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893187
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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