A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915907



Internal ID22691125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87957659..88486238hg38UCSC Ensembl
chr9:90572574..91101153hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38528580
hg19528580
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446513
Samples
Known GenesCDK20, SPATA31C2, SPIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915907
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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