A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438017



Internal ID21095570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128761730..128795415hg38UCSC Ensembl
chr9:131524009..131557694hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3833686
hg1933686
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224764
Samples
Known GenesTBC1D13, ZER1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438017
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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