A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11074011



Internal ID5333273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96617545..96628051hg38UCSC Ensembl
chr3:96336389..96346895hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810507
hg1910507
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597076
Supporting Variants
SamplesNA18873
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11074011
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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