A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427799



Internal ID21085352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4024171..4113875hg38UCSC Ensembl
chr9:4024171..4113875hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3889705
hg1989705
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18217194
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427799
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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