A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2800523



Internal ID21245861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:876934..876934hg38UCSC Ensembl
chr19:876934..876934hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13687758
Samples
Known GenesMED16
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2800523
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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