A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16957235



Internal ID38801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155497928..155498525hg38UCSC Ensembl
chr4:156419080..156419677hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5460245
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16957235
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.128783


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