A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441729



Internal ID21099282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135061502..135070487hg38UCSC Ensembl
chr9:137953348..137962333hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg388986
hg198986
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226086
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441729
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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