A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429346



Internal ID21086899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:13570201..13575900hg38UCSC Ensembl
chr9:13570200..13575899hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg385700
hg195700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176019
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429346
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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