A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431383



Internal ID21088936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29336768..29337341hg38UCSC Ensembl
chr9:29336766..29337339hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg38574
hg19574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185248
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431383
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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