A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707941



Internal ID21229730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111166348..111166348hg38UCSC Ensembl
chr6:111487551..111487551hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg384567
hg194567
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2812648
Supporting Variants
Samples
Known GenesSLC16A10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707941
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.078125


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