A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923759



Internal ID22698986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123638410..123638488hg38UCSC Ensembl
chr9:126400689..126400767hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439517
Samples
Known GenesDENND1A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923759
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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