A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165052



Internal ID20732092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:12985110..13004723hg38UCSC Ensembl
chr8:12842619..12862232hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3819614
hg1919614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418055
Supporting Variants
Samples
Known GenesKIAA1456
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165052
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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