A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643685



Internal ID6683756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:11928944..11935305hg38UCSC Ensembl
chr19:12039759..12046120hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg386362
hg196362
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15991471, essv15991470
SamplesNA20881, HG00109
Known GenesZNF700
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643685
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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