A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17704228



Internal ID127894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64747749..64749390hg38UCSC Ensembl
chr15:65039948..65041589hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg381642
hg191642
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5554885
Supporting Variants
Samples
Known GenesRBPMS2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17704228
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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