A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6110822



Internal ID22020055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94266137..94527227hg38UCSC Ensembl
chr9:97028419..97289509hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38261091
hg19261091
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586173
Samples
Known GenesHIATL1, LOC100132077, NUTM2F, ZNF169
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6110822
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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