A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416991



Internal ID21074544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:24690380..24723966hg38UCSC Ensembl
chr9:24690378..24723964hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3833587
hg1933587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189014
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416991
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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