A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16949974



Internal ID33993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:47620544..47625454hg38UCSC Ensembl
chr4:47622561..47627471hg19UCSC Ensembl
Cytoband4p12
Allele length
AssemblyAllele length
hg384911
hg194911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460944
Supporting Variants
Samples
Known GenesCORIN
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16949974
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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