A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558963



Internal ID332012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:6641748..6641783hg38UCSC Ensembl
chr6:6641981..6642016hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16978060
Samples
Known GenesLY86
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558963
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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