A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173015



Internal ID20740055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:84123634..84132890hg38UCSC Ensembl
chr8:85035869..85045125hg19UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg389257
hg199257
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6421055
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173015
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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