A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256848



Internal ID22061458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91133173..91133173hg38UCSC Ensembl
chr6:91842891..91842891hg19UCSC 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 Variantsnssv17859534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256848
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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