A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961034



Internal ID41330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173347348..173347420hg38UCSC Ensembl
chr4:174268499..174268571hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563591
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961034
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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