A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706596



Internal ID21228388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47592604..47592604hg38UCSC Ensembl
chr1:48058276..48058276hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706596
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.734375


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer