A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588076



Internal ID21780119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131922678..131922757hg38UCSC Ensembl
chr9:134798065..134798144hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014355
Supporting Variants
Samples
Known GenesMED27
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588076
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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