A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17593678



Internal ID21785721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9309520..9309520hg38UCSC Ensembl
chr11:9331067..9331067hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086336
Supporting Variants
Samples
Known GenesTMEM41B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17593678
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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