A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5650459



Internal ID21598764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5863064..5863064hg38UCSC Ensembl
chr17:5766384..5766384hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17086465, nssv17094837
SamplesHG00731, HG00513
Known GenesLOC339166
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5650459
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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