A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17435894



Internal ID22493764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123913683..123919661hg38UCSC Ensembl
chr9:126675962..126681940hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg385979
hg195979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5914675
Supporting Variants
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17435894
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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