A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664912



Internal ID21613219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63101736..63101736hg38UCSC Ensembl
chr20:61733088..61733088hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17117630
SamplesNA12878
Known GenesHAR1A, HAR1B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664912
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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