A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555079



Internal ID328245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104417803..104503929hg38UCSC Ensembl
chr6:104865678..104951804hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3886127
hg1986127
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16987791
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555079
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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