A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5522806



Internal ID9672717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:118465655..118466845hg38UCSC Ensembl
chr10:120225167..120226357hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381191
hg191191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663168
Supporting Variants
SamplesNA19401
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5522806
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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