A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819332



Internal ID21264670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:4735335..4735335hg38UCSC Ensembl
chr9:4735335..4735335hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38124
hg19124
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13704836
Samples
Known GenesAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819332
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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