A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644244



Internal ID7031000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36030267..36044336hg38UCSC Ensembl
chr19:36521169..36535238hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3814070
hg1914070
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16046279, essv16046278
SamplesHG02180, HG02666
Known GenesCLIP3, THAP8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644244
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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