A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140803



Internal ID20707843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27260455..27266434hg38UCSC Ensembl
chr6:27228234..27234213hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg385980
hg195980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404748
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00023


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