A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2674482



Internal ID9940587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:952203..979805hg38UCSC Ensembl
Outerchr10:952166..979855hg38UCSC Ensembl
Innerchr10:998143..1025745hg19UCSC Ensembl
Outerchr10:998106..1025795hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3827690
hg1927690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6374734, essv6130547
SamplesNA19921, NA19435
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2674482
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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