A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015550



Internal ID21924893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:116524888..116553176hg38UCSC Ensembl
chr9:119287167..119315455hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg3828289
hg1928289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17584963
Samples
Known GenesASTN2, LOC100128505
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015550
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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