A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6428959



Internal ID21086512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15163321..15205245hg38UCSC Ensembl
chr9:15163319..15205243hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3841925
hg1941925
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217517
Samples
Known GenesTTC39B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6428959
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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