A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586486



Internal ID21778529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133255280..133255410hg38UCSC Ensembl
chr9:136130667..136130797hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6004708
Supporting Variants
Samples
Known GenesABO
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586486
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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