A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2812413



Internal ID21257751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166997814..166997814hg38UCSC Ensembl
chr6:167411302..167411302hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg381454
hg191454
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703399
Samples
Known GenesMIR3939
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2812413
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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