A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105873



Internal ID22015106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22470990..23124306hg38UCSC Ensembl
chr15:22748962..23400929hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38653317
hg19651968
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17608274
Samples
Known GenesCYFIP1, GOLGA8I, HERC2P2, HERC2P7, LOC283683, NIPA1, NIPA2, TUBGCP5, WHAMMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105873
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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