A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453182



Internal ID21110735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65704901..65743700hg38UCSC Ensembl
chr9:42685821..42724620hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3838800
hg1938800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7807n223
Supporting Variantsnssv18218540
Samples
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453182
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