A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16904540



Internal ID3846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65053126..65201080hg38UCSC Ensembl
chr1:65518809..65666763hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38147955
hg19147955
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556912
Supporting Variants
Samples
Known GenesAK4, MIR101-1, MIR3671
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16904540
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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