A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111103



Internal ID22020336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:99513922..100390410hg38UCSC Ensembl
chr5:98849626..99726114hg19UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg38876489
hg19876489
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547407
Samples
Known GenesLOC100133050
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111103
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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