A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435361



Internal ID21092914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15144338..15146909hg38UCSC Ensembl
chr9:15144336..15146907hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382572
hg192572
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435361
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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