A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17367352



Internal ID22593021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:104554685..109812698hg38UCSC Ensembl
chr10:106314443..111572456hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg385258014
hg195258014
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968492
Supporting Variants
Samples
Known GenesRNU6-53P, SORCS1, SORCS3, SORCS3-AS1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17367352
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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