A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172836



Internal ID20739876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92126631..92127924hg38UCSC Ensembl
chr8:93138859..93140152hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg381294
hg191294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435355
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172836
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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