A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2673024



Internal ID9592443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1026538..1029659hg38UCSC Ensembl
Outerchr10:1026501..1029709hg38UCSC Ensembl
Innerchr10:1072478..1075599hg19UCSC Ensembl
Outerchr10:1072441..1075649hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg383209
hg193209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6076588
SamplesNA18619
Known GenesIDI2-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2673024
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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