A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914661



Internal ID22689878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96356596..96356682hg38UCSC Ensembl
chr9:99118878..99118964hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17431589
Samples
Known GenesSLC35D2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914661
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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