A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425388



Internal ID21082941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:32138854..32150241hg38UCSC Ensembl
chr9:32138852..32150239hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3811388
hg1911388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185794
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425388
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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