A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502320



Internal ID20875564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30576499..30586782hg38UCSC Ensembl
chr16:30587820..30598103hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3810284
hg1910284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029169
Samples
Known GenesZNF785
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502320
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