A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678472



Internal ID21200333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:70126795..70126795hg38UCSC Ensembl
chr11:69972901..69972901hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790463
Supporting Variants
Samples
Known GenesANO1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678472
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.741379


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