A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799214



Internal ID21244552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55456304..55456304hg38UCSC Ensembl
chr19:55967671..55967671hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13695843
Samples
Known GenesISOC2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799214
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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