A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505426



Internal ID20878695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72654900..72705190hg38UCSC Ensembl
chr16:72688799..72739089hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg3850291
hg1950291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505426
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