A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595872



Internal ID6983190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36683963..36703085hg38UCSC Ensembl
chr3:36725454..36744576hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg3819123
hg1919123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10981035
SamplesHG03461
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595872
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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