A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13700552



Internal ID21222391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2099223..2099223hg38UCSC Ensembl
chr5:2099337..2099337hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2811655
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13700552
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.171875


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