A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260236



Internal ID22064846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41046768..41046768hg38UCSC Ensembl
chr5:41046870..41046870hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38277
hg19277
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17855585
Samples
Known GenesMROH2B
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260236
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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