A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6249689



Internal ID22054299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:25643212..25643212hg38UCSC Ensembl
chr14:26112418..26112418hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17845785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6249689
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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