A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595814



Internal ID6983132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:34439621..34589742hg38UCSC Ensembl
chr3:34481113..34631234hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38150122
hg19150122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv883e214
Supporting Variantsessv10979524, essv10979523, essv10979525, essv10979522
SamplesNA19066, HG02262, HG01486, NA18988
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595814
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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