A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173077



Internal ID20740117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89823608..89824054hg38UCSC Ensembl
chr8:90835836..90836282hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38447
hg19447
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6420580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173077
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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