A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17577783



Internal ID21769826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18366691..18366691hg38UCSC Ensembl
chr11:18388238..18388238hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6092832
Supporting Variants
Samples
Known GenesGTF2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17577783
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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