A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16946633



Internal ID31780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:24808992..24810527hg38UCSC Ensembl
chr4:24810614..24812149hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381536
hg191536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5448890
Supporting Variants
Samples
Known GenesCCDC149
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16946633
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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