A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663179



Internal ID9582598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10036035..10043614hg38UCSC Ensembl
Outerchr1:10035878..10043767hg38UCSC Ensembl
Innerchr1:10096093..10103672hg19UCSC Ensembl
Outerchr1:10095936..10103825hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg387890
hg197890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12e199
Supporting Variantsessv6571065, essv5504898
SamplesHG00139, NA11892
Known GenesUBE4B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663179
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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