A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5832849



Internal ID22607784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26039180..26042626hg38UCSC Ensembl
chr2:26262049..26265495hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383447
hg193447
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17484066
Samples
Known GenesRAB10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5832849
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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