A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632789



Internal ID21581094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36223510..36223510hg38UCSC Ensembl
chr9:36223507..36223507hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161734
SamplesNA20509
Known GenesGNE
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632789
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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