A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16958217



Internal ID39458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157369157..157379415hg38UCSC Ensembl
chr4:158290309..158300567hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3810259
hg1910259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16958217
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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