A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5653290



Internal ID21601595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:16127543..16127543hg38UCSC Ensembl
chr17:16030857..16030857hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096690
SamplesNA19238
Known GenesNCOR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5653290
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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