A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428923



Internal ID21086476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15799701..15823200hg38UCSC Ensembl
chr9:15799699..15823198hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3823500
hg1923500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230912
Samples
Known GenesCCDC171
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428923
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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