A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235992



Internal ID20803032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:95600101..95606000hg38UCSC Ensembl
chr6:96047977..96053876hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6400396
Supporting Variants
Samples
Known GenesMANEA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235992
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00016


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