A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6445819



Internal ID9838667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:86215133..86219139hg38UCSC Ensembl
Outerchr1:86214762..86219509hg38UCSC Ensembl
Innerchr1:86680816..86684822hg19UCSC Ensembl
Outerchr1:86680445..86685192hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg384748
hg194748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677907
Supporting Variants
SamplesNA20502
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6445819
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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