A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033431



Internal ID20600471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85918101..85919400hg38UCSC Ensembl
chr16:85951707..85953006hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6514130
Supporting Variants
Samples
Known GenesIRF8, MIR6774
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033431
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer