A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11082663



Internal ID1508797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99230703..99287997hg38UCSC Ensembl
chr3:98949547..99006841hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3857295
hg1957295
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597141
Supporting Variants
SamplesHG01389
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11082663
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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