A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17588938



Internal ID21780981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60672774..60672947hg38UCSC Ensembl
chr9_gl000199_random:154216..154389hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007063
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17588938
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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