A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231547



Internal ID20798588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:92353954..92443658hg38UCSC Ensembl
chr6:93063672..93153376hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3889705
hg1989705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6398375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231547
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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