A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5959029



Internal ID22734074
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121496757..121496757hg38UCSC Ensembl
chr9:124259035..124259035hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17449597
Samples
Known GenesGGTA1P
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5959029
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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