A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16983137



Internal ID56136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41205576..41211574hg38UCSC Ensembl
chr6:41173314..41179312hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg385999
hg195999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5473884
Supporting Variants
Samples
Known GenesTREML3P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16983137
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000468


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