A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163009



Internal ID20730051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:11128412..11133277hg38UCSC Ensembl
chr8:10985922..10990787hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg384866
hg194866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6419815
Supporting Variants
Samples
Known GenesXKR6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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