A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162407



Internal ID20729447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106567201..106569400hg38UCSC Ensembl
chr8:107579429..107581628hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422779
Supporting Variants
Samples
Known GenesOXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162407
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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