A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676570



Internal ID9942675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15497353..15501530hg38UCSC Ensembl
Outerchr10:15497196..15501683hg38UCSC Ensembl
Innerchr10:15539352..15543529hg19UCSC Ensembl
Outerchr10:15539195..15543682hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384488
hg194488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6211981
SamplesNA12889
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676570
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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