A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956637



Internal ID38396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:146808693..146809938hg38UCSC Ensembl
chr4:147729845..147731090hg19UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5454902
Supporting Variants
Samples
Known GenesTTC29
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956637
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.064315


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