A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256837



Internal ID22061447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89807027..89807027hg38UCSC Ensembl
chr6:90516746..90516746hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859525
Samples
Known GenesMDN1
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256837
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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