A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6256866



Internal ID22061476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:93404883..93404883hg38UCSC Ensembl
chr6:94114601..94114601hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17859551
Samples
Known GenesEPHA7
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6256866
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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