A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595870



Internal ID6983188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36670117..36677786hg38UCSC Ensembl
Innerchr3:36670172..36677732hg38UCSC Ensembl
Outerchr3:36670063..36677841hg38UCSC Ensembl
chr3:36711608..36719277hg19UCSC Ensembl
Innerchr3:36711663..36719223hg19UCSC Ensembl
Outerchr3:36711554..36719332hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg387670
hg197670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10981027, essv10981030, essv10981032, essv10981028, essv10981025, essv10981033, essv10981031, essv10981029, essv10981026
SamplesHG02561, HG03225, HG03088, HG03547, NA19118, HG03064, NA18909, HG01254, HG01886
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595870
Frequency
Sample Size2504
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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