A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5854987



Internal ID22629922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:120111881..120113880hg38UCSC Ensembl
chr12:120549685..120551684hg19UCSC Ensembl
Cytoband12q24.23
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17451436
Samples
Known GenesRAB35
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5854987
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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