A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683970



Internal ID21205825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:45208294..45208294hg38UCSC Ensembl
chr22:45604175..45604175hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2804824
Supporting Variants
Samples
Known GenesKIAA0930
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683970
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.28125


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