A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704697



Internal ID21226499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151769287..151769287hg38UCSC Ensembl
chr1:151741763..151741763hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801022
Supporting Variants
Samples
Known GenesOAZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704697
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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