A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445987



Internal ID21103540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36590018..36596427hg38UCSC Ensembl
chr9:36590015..36596424hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg386410
hg196410
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223908
Samples
Known GenesMELK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445987
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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