A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595138



Internal ID6982456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:5535442..5666540hg38UCSC Ensembl
chr3:5577129..5708227hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38131099
hg19131099
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10906750
SamplesNA19334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595138
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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