A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2798726



Internal ID21244064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33218662..33218662hg38UCSC Ensembl
chr19:33709568..33709568hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13680588
Samples
Known GenesSLC7A10
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2798726
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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