A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588222



Internal ID21780265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111848604..111848692hg38UCSC Ensembl
chr9:114610884..114610972hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014380
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588222
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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