A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6250905



Internal ID22055515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:57848866..57848866hg38UCSC Ensembl
chr17:55926227..55926227hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17848885
Samples
Known GenesMRPS23
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6250905
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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