A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100884



Internal ID22010117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:63101736..63101736hg38UCSC Ensembl
chr20:61733088..61733088hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381196
hg191196
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634423
Samples
Known GenesHAR1A, HAR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100884
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer