A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102077



Internal ID22011310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27824160..27831491hg38UCSC Ensembl
chr6:27791938..27799269hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg387332
hg197332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559655
Samples
Known GenesHIST1H4J, HIST1H4K
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102077
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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