A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17365564



Internal ID22591233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92660356..92660356hg38UCSC Ensembl
chr10:94420113..94420113hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5964961
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17365564
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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