A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13702246



Internal ID21224067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:59645322..59645322hg38UCSC Ensembl
chr11:59412795..59412795hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791288
Supporting Variants
Samples
Known GenesPATL1
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13702246
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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