A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644193



Internal ID7030949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33718830..33745191hg38UCSC Ensembl
chr19:34209735..34236096hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3826362
hg1926362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16043760, essv16043761
SamplesNA12762, HG01615
Known GenesCHST8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644193
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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