A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2799599



Internal ID21244937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:31199765..31199765hg38UCSC Ensembl
chr19:31690671..31690671hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13684034, nssv13680621
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2799599
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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