A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16950375



Internal ID34272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65141900..65145809hg38UCSC Ensembl
chr4:66007618..66011527hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg383910
hg193910
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560708
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16950375
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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