A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17586897



Internal ID21778940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92674405..93060540hg38UCSC Ensembl
chr10:94434162..94820297hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38386136
hg19386136
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103771
Supporting Variants
Samples
Known GenesEXOC6, HHEX
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17586897
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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