A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665031



Internal ID9584450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51926411..51927130hg38UCSC Ensembl
Outerchr10:51926374..51927180hg38UCSC Ensembl
Innerchr10:53686171..53686890hg19UCSC Ensembl
Outerchr10:53686134..53686940hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38807
hg19807
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6057349
SamplesNA20520
Known GenesPRKG1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665031
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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