A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907415



Internal ID5731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75669247..75673027hg38UCSC Ensembl
chr1:76134932..76138712hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg383781
hg193781
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907415
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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