A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16945560



Internal ID31036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:16736742..16736745hg38UCSC Ensembl
chr4:16738365..16738368hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5403785
Supporting Variants
Samples
Known GenesLDB2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16945560
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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