A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5399802



Internal ID179188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63715968..63716019hg38UCSC Ensembl
chr6:64425864..64425915hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38240
hg19240
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735534
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5399802
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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