A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5955961



Internal ID9707534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11841914..11843834hg38UCSC Ensembl
chr8:11699423..11701343hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381921
hg191921
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668269
Supporting Variants
SamplesNA19457
Known GenesCTSB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5955961
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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