A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169054



Internal ID20736094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:54372687..54378359hg38UCSC Ensembl
chr8:55285247..55290919hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg385673
hg195673
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430280
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169054
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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