A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685755



Internal ID21207616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31203676..31203676hg38UCSC Ensembl
chr4:31205298..31205298hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38404
hg19404
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2810939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685755
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.515625


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