A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002560



Internal ID21911903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74655422..74657145hg38UCSC Ensembl
chr9:77270338..77272061hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381724
hg191724
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17589653
Samples
Known GenesRORB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002560
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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