A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142298



Internal ID20709338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:164262066..164273466hg38UCSC Ensembl
chr6:164683099..164694499hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3811401
hg1911401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600160
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142298
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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