A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920984



Internal ID22696207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:3934429..3935409hg38UCSC Ensembl
chr9:3934429..3935409hg19UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg38981
hg19981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17446944
Samples
Known GenesGLIS3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920984
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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