A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675721



Internal ID9941826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18771896..18980140hg38UCSC Ensembl
chr10:19060825..19269069hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38208245
hg19208245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6178622
SamplesNA19334
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675721
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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