A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704737



Internal ID21226539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37808749..37808749hg38UCSC Ensembl
chr9:37808746..37808746hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2818798
Supporting Variants
Samples
Known GenesDCAF10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704737
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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