A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16962566



Internal ID42356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10906313..10907996hg38UCSC Ensembl
chr5:10906425..10908108hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563759
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16962566
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.001093


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