A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11066212



Internal ID6033019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:87905505..87959581hg38UCSC Ensembl
chr3:87954655..88008731hg19UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3854077
hg1954077
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596907
Supporting Variants
SamplesNA19438
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11066212
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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