A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956603



Internal ID38379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146408337..146411704hg38UCSC Ensembl
chr4:147329489..147332856hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg383368
hg193368
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466217
Supporting Variants
Samples
Known GenesMIR7849, SLC10A7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956603
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000937


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