A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13676625



Internal ID21198475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:67043927..67043927hg38UCSC Ensembl
chr10:68803685..68803685hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381541
hg191541
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2789368
Supporting Variants
Samples
Known GenesCTNNA3, LRRTM3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13676625
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.109375


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