A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6247585



Internal ID22052195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:117521473..117521473hg38UCSC Ensembl
chr10:119280984..119280984hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17842276
Samples
Known GenesEMX2OS
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6247585
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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