A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5405770



Internal ID185112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:5819487..5819538hg38UCSC Ensembl
chr6:5819720..5819771hg19UCSC Ensembl
Cytoband6p25.1
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 Variantsnssv16978486
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5405770
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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