A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169804



Internal ID20736844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:63232306..63232557hg38UCSC Ensembl
chr8:64144864..64145115hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416786
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0207


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