A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867380



Internal ID22642315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137908314..137925038hg38UCSC Ensembl
chr9:140802766..140819490hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3816725
hg1916725
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17511845
Samples
Known GenesCACNA1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867380
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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