A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662058



Internal ID21610363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78558447..78558447hg38UCSC Ensembl
chr17:76554529..76554529hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081139
SamplesHG03486
Known GenesDNAH17
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662058
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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