A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165109



Internal ID20732149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:130892448..130896740hg38UCSC Ensembl
chr8:131904694..131908986hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg384293
hg194293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415988
Supporting Variants
Samples
Known GenesADCY8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165109
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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