A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2818949



Internal ID21264288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66376333..66376333hg38UCSC Ensembl
chr8:67288568..67288568hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38115
hg19115
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705167
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2818949
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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