A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437052



Internal ID21094605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:131240901..131472900hg38UCSC Ensembl
chr9:134116288..134348287hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg38232000
hg19232000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224081
Samples
Known GenesFAM78A, PPAPDC3, PRRC2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437052
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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