A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562344



Internal ID335302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:92266854..92881037hg38UCSC Ensembl
chr9:95029136..95643319hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg38614184
hg19614184
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027405
Samples
Known GenesANKRD19P, ASPN, BICD2, CENPP, ECM2, IARS, IPPK, LOC100128361, MIR3651, MIR4670, NOL8, OGN, OMD, SNORA84, ZNF484
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562344
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer