A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171765



Internal ID20738805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93765706..93766021hg38UCSC Ensembl
chr8:94777934..94778249hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422909
Supporting Variants
Samples
Known GenesTMEM67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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