A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436606



Internal ID21094159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104345409..104414188hg38UCSC Ensembl
chr9:107107690..107176469hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3868780
hg1968780
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230225
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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