A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959914



Internal ID40585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:165598006..165598015hg38UCSC Ensembl
chr4:166519158..166519167hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5547051
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959914
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.085612


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