A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102499



Internal ID22011734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50914499..50914499hg38UCSC Ensembl
chr20:49531036..49531036hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631212
Samples
Known GenesADNP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102499
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