A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453589



Internal ID21111142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36569947..36579305hg38UCSC Ensembl
chr9:36569944..36579302hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg389359
hg199359
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178518
Samples
Known GenesMELK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453589
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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