A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13684158



Internal ID21206015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130013973..130013973hg38UCSC Ensembl
chr10:131812237..131812237hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2788261
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13684158
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.296875


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