A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692800



Internal ID21214652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36688500..36688500hg38UCSC Ensembl
chr1:37154101..37154101hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801848
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692800
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