A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418312



Internal ID21075865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:18427799..18428543hg38UCSC Ensembl
chr9:18427797..18428541hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg38745
hg19745
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418312
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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