A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11161154



Internal ID2133382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:139899625..139903083hg38UCSC Ensembl
Innerchr3:139899663..139903046hg38UCSC Ensembl
Outerchr3:139899588..139903121hg38UCSC Ensembl
chr3:139618467..139621925hg19UCSC Ensembl
Innerchr3:139618505..139621888hg19UCSC Ensembl
Outerchr3:139618430..139621963hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg383459
hg193459
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597942
Supporting Variants
SamplesHG01936
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11161154
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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