A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10979740



Internal ID3719666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:35304282..35332401hg38UCSC Ensembl
Innerchr3:35304282..35332401hg38UCSC Ensembl
Outerchr3:35303782..35332901hg38UCSC Ensembl
chr3:35345774..35373893hg19UCSC Ensembl
Innerchr3:35345774..35373893hg19UCSC Ensembl
Outerchr3:35345274..35374393hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3828120
hg1928120
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595830
Supporting Variants
SamplesHG03351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10979740
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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