A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5644923



Internal ID21593228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38448801..38448801hg38UCSC Ensembl
chr17:36605045..36605045hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17081396
SamplesNA19238
Known GenesARHGAP23
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5644923
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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