A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631970



Internal ID21580275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82909776..82909776hg38UCSC Ensembl
chr9:85524691..85524691hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17162701
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631970
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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