A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17601865



Internal ID21793912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:130294410..130294410hg38UCSC Ensembl
chr11:130164305..130164305hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg382456
hg192456
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6089409
Supporting Variants
Samples
Known GenesZBTB44
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17601865
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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