A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426458



Internal ID21084011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19145052..19209859hg38UCSC Ensembl
chr9:19145050..19209857hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3864808
hg1964808
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7636n223
Supporting Variantsnssv18175541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426458
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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