A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16991118



Internal ID61485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161115488..161115534hg38UCSC Ensembl
chr6:161536520..161536566hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5396309
Supporting Variants
Samples
Known GenesMAP3K4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16991118
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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