A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111935



Internal ID22021168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92463614..92464221hg38UCSC Ensembl
chr8:93475842..93476449hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17579313
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111935
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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