A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6450294



Internal ID21107847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:34181608..34194475hg38UCSC Ensembl
chr9:34181606..34194473hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3812868
hg1912868
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183341
Samples
Known GenesUBAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6450294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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