A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5609609



Internal ID21557914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:94633155..94633155hg38UCSC Ensembl
chr9:42595803..42595803hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg38933
hg19933
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17115274
SamplesNA19240
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5609609
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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