A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676037



Internal ID9942142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5861867..5864757hg38UCSC Ensembl
chr10:5903830..5906720hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg382891
hg192891
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5790546, essv5797483
SamplesNA19904, NA18868
Known GenesANKRD16
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676037
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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