A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4755997



Internal ID20531857
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 StatusM
Merged Variantsdgv13n199
Supporting Variantsnssv16287044
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)nsv4755997
Frequency
Sample Size25
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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