A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17702168



Internal ID125834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:77975462..78778174hg38UCSC Ensembl
chr15:78267804..79070516hg19UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg38802713
hg19802713
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556515
Supporting Variants
Samples
Known GenesACSBG1, ADAMTS7, CHRNA3, CHRNA5, CHRNB4, CIB2, CRABP1, DNAJA4, HYKK, IDH3A, IREB2, LOC646938, LOC91450, MIR5003, PSMA4, SH2D7, TBC1D2B, WDR61
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17702168
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.010771


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