A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13688632



Internal ID21210448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39507491..39507491hg38UCSC Ensembl
chr13:40081628..40081628hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792689
Supporting Variants
Samples
Known GenesLHFP
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13688632
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.921875


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