A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420036



Internal ID21077589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:17629544..17647677hg38UCSC Ensembl
chr9:17629542..17647675hg19UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3818134
hg1918134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234373
Samples
Known GenesSH3GL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420036
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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