A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13687933



Internal ID21209788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47686734..47686734hg38UCSC Ensembl
chr1:48152406..48152406hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801243
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13687933
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0645161


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