A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639761



Internal ID21588066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123405649..123405649hg38UCSC Ensembl
chr9:126167928..126167928hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg38187
hg19187
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17159915
SamplesHG03486
Known GenesDENND1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639761
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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