A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962369



Internal ID42212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187940822..188765960hg38UCSC Ensembl
chr4:188861976..189687114hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38825139
hg19825139
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5557707
Supporting Variants
Samples
Known GenesLINC01060, TRIML1, TRIML2, ZFP42
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962369
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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