A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217435



Internal ID20784475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:85854740..85867550hg38UCSC Ensembl
chr6:86564458..86577268hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3812811
hg1912811
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407218
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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