A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169323



Internal ID20736363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:64989401..64991700hg38UCSC Ensembl
chr8:65901636..65903935hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422831
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169323
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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