A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162622



Internal ID20729662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:10339830..10358782hg38UCSC Ensembl
chr8:10197340..10216292hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3818953
hg1918953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430249
Supporting Variants
Samples
Known GenesMSRA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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