A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2816848



Internal ID21262186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99675634..99675634hg38UCSC Ensembl
chr7:99273257..99273257hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38190
hg19190
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13705538
Samples
Known GenesCYP3A5
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2816848
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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