A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530205



Internal ID20903566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:18556659..18563794hg38UCSC Ensembl
chr20:18537303..18544438hg19UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg387136
hg197136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18067312
Samples
Known GenesSEC23B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530205
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