A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260880



Internal ID22065490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:77939703..77939703hg38UCSC Ensembl
chr6:78649420..78649420hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17857395
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260880
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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