A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6260179



Internal ID22064789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:34837678..34837678hg38UCSC Ensembl
chr5:34837783..34837783hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17856974
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6260179
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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