A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6257362



Internal ID22061972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:152139707..152139707hg38UCSC Ensembl
chr6:152460842..152460842hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859892
Samples
Known GenesSYNE1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6257362
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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