A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596534



Internal ID6983849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72130860..72131352hg38UCSC Ensembl
Innerchr3:72130862..72131351hg38UCSC Ensembl
Outerchr3:72130859..72131354hg38UCSC Ensembl
chr3:72180011..72180503hg19UCSC Ensembl
Innerchr3:72180013..72180502hg19UCSC Ensembl
Outerchr3:72180010..72180505hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38493
hg19493
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11038616
SamplesHG01079
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596534
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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