A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683331



Internal ID21205192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66400522..66400522hg38UCSC Ensembl
chr1:66866205..66866205hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2802562
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683331
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