A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10903653



Internal ID905469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4100672..4218932hg38UCSC Ensembl
Innerchr3:4100688..4218917hg38UCSC Ensembl
Outerchr3:4100657..4218948hg38UCSC Ensembl
chr3:4142356..4260616hg19UCSC Ensembl
Innerchr3:4142372..4260601hg19UCSC Ensembl
Outerchr3:4142341..4260632hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38118261
hg19118261
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595087
Supporting Variants
SamplesNA20502
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10903653
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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