A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5645567



Internal ID21593872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31859356..31859356hg38UCSC Ensembl
chr17:30186375..30186375hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17091624
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5645567
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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