A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643893



Internal ID6683962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20638487..20665457hg38UCSC Ensembl
chr19:20821293..20848263hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3826971
hg1926971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16009683
SamplesHG01363
Known GenesZNF626
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643893
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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