A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5659865



Internal ID21608170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67268455..67268455hg38UCSC Ensembl
chr17:65264571..65264571hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17084837
SamplesHG00733
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5659865
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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