A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17618916



Internal ID21810963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39922709..39922709hg38UCSC Ensembl
chr17:38078962..38078962hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091267
Supporting Variants
Samples
Known GenesORMDL3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17618916
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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