A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819688



Internal ID21265026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:60647619..60647619hg38UCSC Ensembl
chr9_gl000199_random:129061..129061hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697524
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819688
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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