A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169518



Internal ID20736558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:69871307..69875740hg38UCSC Ensembl
chr8:70783542..70787975hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg384434
hg194434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426656
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169518
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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