A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16896483



Internal ID171798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16026617..16048527hg38UCSC Ensembl
chr1:16353112..16375022hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821911
hg1921911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5427283
Supporting Variants
Samples
Known GenesCLCNKA, CLCNKB
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16896483
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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