A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10903635



Internal ID905451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4100349..4167284hg38UCSC Ensembl
Innerchr3:4100365..4167269hg38UCSC Ensembl
Outerchr3:4100334..4167300hg38UCSC Ensembl
chr3:4142033..4208968hg19UCSC Ensembl
Innerchr3:4142049..4208953hg19UCSC Ensembl
Outerchr3:4142018..4208984hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3866936
hg1966936
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595086
Supporting Variants
SamplesHG03518
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10903635
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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