A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173585



Internal ID20740625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9890872..9892491hg38UCSC Ensembl
chr8:9748382..9750001hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381620
hg191620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173585
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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