A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5626953



Internal ID21575258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123577669..123577669hg38UCSC Ensembl
chr9:126339948..126339948hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160280
SamplesNA19239
Known GenesDENND1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5626953
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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