A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5662587



Internal ID21610892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35593621..35593621hg38UCSC Ensembl
chr17:33920640..33920640hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38737
hg19737
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087268
SamplesHG03732
Known GenesAP2B1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5662587
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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