A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656336



Internal ID21604641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:49295410..49295410hg38UCSC Ensembl
chr17:47372772..47372772hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087166
SamplesHG03683
Known GenesZNF652
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656336
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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