A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10903616



Internal ID905432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4092194..4130816hg38UCSC Ensembl
Innerchr3:4092694..4130316hg38UCSC Ensembl
Outerchr3:4091194..4131816hg38UCSC Ensembl
chr3:4133878..4172500hg19UCSC Ensembl
Innerchr3:4134378..4172000hg19UCSC Ensembl
Outerchr3:4132878..4173500hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3838623
hg1938623
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595084
Supporting Variants
SamplesNA20542
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10903616
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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