A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526445



Internal ID20899806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:20363401..20370100hg38UCSC Ensembl
chr20:20344045..20350744hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203205
Samples
Known GenesINSM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526445
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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