A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17465097



Internal ID22522986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92845850..92854019hg38UCSC Ensembl
chr10:94605607..94613776hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg388170
hg198170
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5852843
Supporting Variants
Samples
Known GenesEXOC6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17465097
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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