A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430048



Internal ID21087601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3934429..3935420hg38UCSC Ensembl
chr9:3934429..3935420hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194453
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430048
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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