A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504155



Internal ID20877416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:71352616..71436646hg38UCSC Ensembl
chr16:71386519..71470549hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3884031
hg1984031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031945
Samples
Known GenesCALB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504155
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