A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103724



Internal ID22012957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53269009..53269009hg38UCSC Ensembl
chr20:51885548..51885548hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17623833
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103724
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