A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171834



Internal ID20738874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:94876674..94877219hg38UCSC Ensembl
chr8:95888902..95889447hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429987
Supporting Variants
Samples
Known GenesINTS8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171834
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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