A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596552



Internal ID6983866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:73094083..73095940hg38UCSC Ensembl
Innerchr3:73094133..73095890hg38UCSC Ensembl
Outerchr3:73094033..73095990hg38UCSC Ensembl
chr3:73143234..73145091hg19UCSC Ensembl
Innerchr3:73143284..73145041hg19UCSC Ensembl
Outerchr3:73143184..73145141hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381858
hg191858
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11038913
SamplesNA19404
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596552
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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