A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16981567



Internal ID55070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39322533..39330361hg38UCSC Ensembl
chr6:39290309..39298137hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg387829
hg197829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470406
Supporting Variants
Samples
Known GenesKCNK16
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16981567
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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