A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5483169



Internal ID260611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137443360..137445260hg38UCSC Ensembl
chr9:140337812..140339712hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17029701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5483169
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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