A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6100699



Internal ID22009932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:544532..544532hg38UCSC Ensembl
chr20:525176..525176hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17619109
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6100699
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