A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6102438



Internal ID22011673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:87919061..88141042hg38UCSC Ensembl
chr9:90533976..90755957hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg38221982
hg19221982
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17583741
Samples
Known GenesCDK20, SPATA31C1, SPATA31C2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6102438
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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