A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16989950



Internal ID60714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:150546303..150546346hg38UCSC Ensembl
chr6:150867439..150867482hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547777
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16989950
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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