A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17484066



Internal ID22541974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:26039180..26042626hg38UCSC Ensembl
chr2:26262049..26265495hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg383447
hg193447
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832849
Supporting Variants
Samples
Known GenesRAB10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17484066
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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