A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5632628



Internal ID21580933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:33569919..33569919hg38UCSC Ensembl
chr9:33569917..33569917hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38575
hg19575
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161952
SamplesNA18939
Known GenesANKRD18B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5632628
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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