A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226180



Internal ID20793220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:99587401..99595400hg38UCSC Ensembl
chr6:100035277..100043276hg19UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603814
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226180
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00081


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