A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670932



Internal ID21619237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50609943..50609943hg38UCSC Ensembl
chr20:49226480..49226480hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17116811
SamplesHG03125
Known GenesFAM65C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670932
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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