A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677432



Internal ID9596851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:84367285..84368359hg38UCSC Ensembl
Outerchr1:84367248..84368409hg38UCSC Ensembl
Innerchr1:84832968..84834042hg19UCSC Ensembl
Outerchr1:84832931..84834092hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6214384
SamplesNA19682
Known GenesUOX
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677432
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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