A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5401520



Internal ID180897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132075660..132075711hg38UCSC Ensembl
chr9:134951047..134951098hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029958
Samples
Known GenesMED27
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5401520
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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