A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16956728



Internal ID38458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:126684217..126814905hg38UCSC Ensembl
chr4:127605372..127736060hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg38130689
hg19130689
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5463715
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16956728
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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