A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16944643



Internal ID30439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27400..231000hg38UCSC Ensembl
chr4:27400..224789hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38203601
hg19197390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5440338
Supporting Variants
Samples
Known GenesZNF595, ZNF718, ZNF876P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16944643
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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