A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5656347



Internal ID21604652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46730796..46730796hg38UCSC Ensembl
chr11:46752346..46752346hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17074672
SamplesNA20847
Known GenesF2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5656347
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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