A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18219682



Internal ID20786722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:51595501..51601100hg38UCSC Ensembl
chr6:51460299..51465898hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400225
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18219682
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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