A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448446



Internal ID21105999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:99903601..99909100hg38UCSC Ensembl
chr9:102665883..102671382hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227566
Samples
Known GenesLOC441461, STX17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448446
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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