A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416008



Internal ID21073561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:26141528..26141882hg38UCSC Ensembl
chr9:26141526..26141880hg19UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38355
hg19355
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185222
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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