A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18162256



Internal ID20729296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105152301..105153200hg38UCSC Ensembl
chr8:106164529..106165428hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422832
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18162256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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