A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16952483



Internal ID35682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:78639285..78641454hg38UCSC Ensembl
chr4:79560439..79562608hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg382170
hg192170
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563473
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16952483
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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