A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562515



Internal ID335468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166069861..166079058hg38UCSC Ensembl
chr6:166483349..166492546hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg389198
hg199198
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990971
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562515
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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