A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440689



Internal ID21098242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:122901501..122910300hg38UCSC Ensembl
chr9:125663780..125672579hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225662
Samples
Known GenesRC3H2, ZBTB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440689
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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