A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686094



Internal ID21207948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:45710734..45710734hg38UCSC Ensembl
chr1:46176406..46176406hg19UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801966
Supporting Variants
Samples
Known GenesIPP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686094
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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