A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16260538



Internal ID20469756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26570660..27316833hg38UCSC Ensembl
chr10:26859589..27605762hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38746174
hg19746174
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756180
Supporting Variants
Samples
Known GenesABI1, ACBD5, ANKRD26, LINC00202-1, LINC00202-2, LINC00264, LRRC37A6P, MASTL, PDSS1, YME1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16260538
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer