A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5397408



Internal ID176814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15995650..15995701hg38UCSC Ensembl
chr6:15995881..15995932hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979079
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5397408
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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