A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952113



Internal ID35432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71079824..71090220hg38UCSC Ensembl
chr4:71945541..71955937hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3810397
hg1910397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455316
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952113
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.003592


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