A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11074701



Internal ID3902668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:97311314..97326804hg38UCSC Ensembl
chr3:97030158..97045648hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3815491
hg1915491
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597093
Supporting Variants
SamplesHG03558
Known GenesEPHA6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11074701
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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