A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670379



Internal ID9589798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:61794280..61798010hg38UCSC Ensembl
Outerchr1:61794243..61798060hg38UCSC Ensembl
Innerchr1:62259952..62263682hg19UCSC Ensembl
Outerchr1:62259915..62263732hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg383818
hg193818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5679815
SamplesNA19777
Known GenesINADL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670379
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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