A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5891774



Internal ID22666816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39308182..39317195hg38UCSC Ensembl
chr6:39275958..39284971hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg389014
hg199014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449254
Samples
Known GenesKCNK16, KCNK17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5891774
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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