A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5630401



Internal ID21578706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:123495141..123495141hg38UCSC Ensembl
chr9:126257420..126257420hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17160276
SamplesNA19650
Known GenesDENND1A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5630401
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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