A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11026102



Internal ID4020767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:61383158..61432945hg38UCSC Ensembl
chr3:61368832..61418619hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3849788
hg1949788
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596340
Supporting Variants
SamplesHG03673
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11026102
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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