A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538963



Internal ID313978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134992271..134992305hg38UCSC Ensembl
chr9:137884117..137884151hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17031217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538963
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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