A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427373



Internal ID21084926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3174932..3192501hg38UCSC Ensembl
chr9:3174932..3192501hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3817570
hg1917570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193836
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427373
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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