A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4756180



Internal ID20532040
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 StatusM
Merged Variantsdgv13n199
Supporting Variantsnssv16260538
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)nsv4756180
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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