A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10903668



Internal ID905484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4130643..4271936hg38UCSC Ensembl
Innerchr3:4130655..4271925hg38UCSC Ensembl
Outerchr3:4130632..4271948hg38UCSC Ensembl
chr3:4172327..4313620hg19UCSC Ensembl
Innerchr3:4172339..4313609hg19UCSC Ensembl
Outerchr3:4172316..4313632hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38141294
hg19141294
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595089
Supporting Variants
SamplesHG02221
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10903668
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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