A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17582793



Internal ID21774836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129234072..129245209hg38UCSC Ensembl
chr9:131996351..132007488hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3811138
hg1911138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020176
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17582793
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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