A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643892



Internal ID6683961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20638487..20665457hg38UCSC Ensembl
chr19:20821293..20848263hg19UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg3826971
hg1926971
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16009681, essv16009682, essv16009680
SamplesHG03663, HG03846, HG02728
Known GenesZNF626
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643892
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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