A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5554991



Internal ID328159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:96253603..96253615hg38UCSC Ensembl
chr6:96701479..96701491hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3813
hg1913
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985553
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5554991
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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