A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16287044



Internal ID20496262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26600555..27316835hg38UCSC Ensembl
chr10:26889484..27605764hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38716281
hg19716281
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4755997
Supporting Variants
Samples
Known GenesABI1, ACBD5, ANKRD26, LINC00202-1, LINC00202-2, LRRC37A6P, MASTL, PDSS1, YME1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16287044
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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