A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6459768



Internal ID21117321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28226601..28228400hg38UCSC Ensembl
chr12:28379534..28381333hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6459768
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