A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6259363



Internal ID22063973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37641928..37641928hg38UCSC Ensembl
chr18:35221891..35221891hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17849290
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6259363
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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