A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423668



Internal ID21081221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17808527..17900804hg38UCSC Ensembl
chr9:17808525..17900802hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3892278
hg1992278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18174826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423668
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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