A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476297



Internal ID253911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95712673..95717040hg38UCSC Ensembl
chr9:98474955..98479322hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg384368
hg194368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17027488
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476297
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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