A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16969016



Internal ID46670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124745949..124746082hg38UCSC Ensembl
chr6:125067095..125067228hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5457897
Supporting Variants
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16969016
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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