A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13683144



Internal ID21205001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195110274..195110274hg38UCSC Ensembl
chr3:194831003..194831003hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38276
hg19276
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2808939
Supporting Variants
Samples
Known GenesXXYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13683144
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.961538


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