A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559469



Internal ID332502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27807584..27815280hg38UCSC Ensembl
chr6:27775362..27783058hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg387697
hg197697
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16980887
Samples
Known GenesHIST1H2AI, HIST1H2AJ, HIST1H2BL, HIST1H2BM, HIST1H3H
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559469
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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