A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3586646



Internal ID6974164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:83588254..83591863hg38UCSC Ensembl
Innerchr1:83588274..83591843hg38UCSC Ensembl
Outerchr1:83588234..83591883hg38UCSC Ensembl
chr1:84053937..84057546hg19UCSC Ensembl
Innerchr1:84053957..84057526hg19UCSC Ensembl
Outerchr1:84053917..84057566hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg383610
hg193610
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9996334
SamplesHG03772
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3586646
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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