A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2796664



Internal ID21242002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28224007..28224007hg38UCSC Ensembl
chr17:26551033..26551033hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38340
hg19340
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13689275
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2796664
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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