A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5492596



Internal ID269805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:5672602..5673382hg38UCSC Ensembl
chr9:5672602..5673382hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17021011
Samples
Known GenesKIAA1432
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5492596
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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