A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5478068



Internal ID255632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:2722257..2722524hg38UCSC Ensembl
chr9:2722257..2722524hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17019399
Samples
Known GenesKCNV2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5478068
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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