A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467285



Internal ID245104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:15207455..15225024hg38UCSC Ensembl
chr6:15207686..15225255hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3817570
hg1917570
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979692
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467285
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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