A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558356



Internal ID331421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:29437544..29438789hg38UCSC Ensembl
chr6:29405321..29406566hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381246
hg191246
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982464
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558356
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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