A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596515



Internal ID6983830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70447272..70454177hg38UCSC Ensembl
Innerchr3:70447772..70453677hg38UCSC Ensembl
Outerchr3:70446272..70455177hg38UCSC Ensembl
chr3:70496423..70503328hg19UCSC Ensembl
Innerchr3:70496923..70502828hg19UCSC Ensembl
Outerchr3:70495423..70504328hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg386906
hg196906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11038182
SamplesHG02589
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596515
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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