A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5639960



Internal ID21588265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32845592..32845592hg38UCSC Ensembl
chr9:32845590..32845590hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17161610
SamplesHG02818
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5639960
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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