A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2817539



Internal ID21262877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109337069..109337069hg38UCSC Ensembl
chr8:110349298..110349298hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13699882
Samples
Known GenesENY2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2817539
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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