A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17841560



Internal ID22025203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123739598..123739598hg38UCSC Ensembl
chr9:126501877..126501877hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6240220
Supporting Variants
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nssv17841560
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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