A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526242



Internal ID20899603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5321620..5324870hg38UCSC Ensembl
chr20:5302266..5305516hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg383251
hg193251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18068241
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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