A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983975



Internal ID56699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83333931..83339990hg38UCSC Ensembl
chr6:84043650..84049709hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg386060
hg196060
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466220
Supporting Variants
Samples
Known GenesME1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983975
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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