A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18170333



Internal ID20737373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:72636801..72645800hg38UCSC Ensembl
chr8:73549036..73558035hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg389000
hg199000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432398
Supporting Variants
Samples
Known GenesKCNB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18170333
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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