A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597942



Internal ID6985079
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11161154
SamplesHG01936
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597942
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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