A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699679



Internal ID21221513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:113900752..113900752hg38UCSC Ensembl
chr9:116663032..116663032hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817297
Supporting Variants
Samples
Known GenesZNF618
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699679
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.666667


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