A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16947413



Internal ID32309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37659515..37660206hg38UCSC Ensembl
chr4:37661137..37661828hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38692
hg19692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5459809
Supporting Variants
Samples
Known GenesRELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16947413
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001093


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