A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586288



Internal ID6973809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65705250..65707354hg38UCSC Ensembl
Innerchr1:65705250..65707354hg38UCSC Ensembl
Outerchr1:65705168..65707421hg38UCSC Ensembl
chr1:66170933..66173037hg19UCSC Ensembl
Innerchr1:66170933..66173037hg19UCSC Ensembl
Outerchr1:66170851..66173104hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382105
hg192105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9958766
SamplesNA19374
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586288
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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