A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5918369



Internal ID22693590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76467302..76468156hg38UCSC Ensembl
chr9:79082218..79083072hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17435774
Samples
Known GenesGCNT1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5918369
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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