A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593146



Internal ID21785189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9465256..9465443hg38UCSC Ensembl
chr11:9486803..9486990hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6027662
Supporting Variants
Samples
Known GenesZNF143
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593146
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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