A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169452



Internal ID20736492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73810801..73812400hg38UCSC Ensembl
chr8:74723036..74724635hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6417969
Supporting Variants
Samples
Known GenesUBE2W
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169452
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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