A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6244610



Internal ID22049220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:102761167..102761167hg38UCSC Ensembl
chr5:102096871..102096871hg19UCSC Ensembl
Cytoband5q21.1
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 Variantsnssv17857858
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferencePrakrithi_et_al_2022
Pubmed ID35178516
Accession Number(s)nsv6244610
Frequency
Sample Size1021
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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