A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502985



Internal ID20876234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:83723356..83734342hg38UCSC Ensembl
chr16:83756961..83767947hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3810987
hg1910987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032479
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502985
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