A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16960005



Internal ID40642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:168043588..168644848hg38UCSC Ensembl
chr4:168964739..169565999hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg38601261
hg19601261
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466965
Supporting Variants
Samples
Known GenesANXA10, DDX60, DDX60L, PALLD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16960005
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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