A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13686831



Internal ID21208685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:68929869..68929869hg38UCSC Ensembl
chr11:68697337..68697337hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38192
hg19192
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2791316
Supporting Variants
Samples
Known GenesIGHMBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13686831
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.296875


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