A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595812



Internal ID6983130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34419757..34576706hg38UCSC Ensembl
chr3:34461249..34618198hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38156950
hg19156950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv883e214
Supporting Variantsessv10979518, essv10979517, essv10979516, essv10979519
SamplesNA19066, HG02262, HG01486, HG01344
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595812
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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