A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18073084



Internal ID20640124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:46270337..46270810hg38UCSC Ensembl
chr21:47690251..47690724hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38474
hg19474
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540406
Supporting Variants
Samples
Known GenesMCM3AP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18073084
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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