A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13699223



Internal ID21221070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15742682..15742682hg38UCSC Ensembl
chr3:15784189..15784189hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38749
hg19749
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2807965
Supporting Variants
Samples
Known GenesANKRD28
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13699223
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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