A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18171519



Internal ID20738559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:99977304..99981746hg38UCSC Ensembl
chr8:100989532..100993974hg19UCSC Ensembl
Cytoband8q22.2
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6429202
Supporting Variants
Samples
Known GenesRGS22
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18171519
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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