A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7961n223



Internal ID22810929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136769701..136807700hg38UCSC Ensembl
chr9:139664153..139702152hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3838000
hg1938000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6438199, nsv6447606, nsv6450226
Samples
Known GenesCCDC183, CCDC183-AS1, TMEM141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7961n223
Frequency
Sample Size19652
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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