A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13694413



Internal ID21216265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:29105015..29105113hg38UCSC Ensembl
chr11:29126562..29126660hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13694413
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.203125


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