A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5480525



Internal ID258032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:7071815..7073152hg38UCSC Ensembl
chr9:7071815..7073152hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg381338
hg191338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17019004
Samples
Known GenesKDM4C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5480525
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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