A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698264



Internal ID21220064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70516302..70516404hg38UCSC Ensembl
chr4:71382019..71382121hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810705
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698264
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.421875


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