A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441096



Internal ID21098649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:126746401..126832100hg38UCSC Ensembl
chr9:129508680..129594379hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3885700
hg1985700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227630
Samples
Known GenesZBTB43
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441096
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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