A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18142842



Internal ID20709882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:33512158..33515429hg38UCSC Ensembl
chr6:33479935..33483206hg19UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg383272
hg193272
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407503
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18142842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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