A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5646572



Internal ID21594877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:27826356..27826356hg38UCSC Ensembl
chr17:26153382..26153382hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081069
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5646572
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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