A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5655264



Internal ID21603569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:46777891..46777891hg38UCSC Ensembl
chr17:44855257..44855257hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17087873
SamplesHG03732
Known GenesWNT3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5655264
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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