A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17027405



Internal ID85987
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 StatusS
Merged Variantsnsv5562344
Supporting Variants
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)nssv17027405
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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