A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16980657



Internal ID54483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15656525..15658390hg38UCSC Ensembl
chr6:15656756..15658621hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381866
hg191866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457221
Supporting Variants
Samples
Known GenesDTNBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16980657
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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