A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689352



Internal ID21211207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6742593..6742593hg38UCSC Ensembl
chr1:6802653..6802653hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg381836
hg191836
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802568
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689352
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.862069


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