A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163991



Internal ID20731031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122836160..122840427hg38UCSC Ensembl
chr8:123848399..123852666hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg384268
hg194268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415770
Supporting Variants
Samples
Known GenesZHX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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