A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444160



Internal ID21101713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135419258..135472007hg38UCSC Ensembl
chr9:138311104..138363853hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3852750
hg1952750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232327
Samples
Known GenesPPP1R26-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444160
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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