A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438199



Internal ID21095752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136770601..136803800hg38UCSC Ensembl
chr9:139665053..139698252hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3833200
hg1933200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7961n223
Supporting Variantsnssv18218606
Samples
Known GenesCCDC183, TMEM141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438199
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