A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704836



Internal ID21226640
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 StatusS
Merged Variantsnsv2819332
Supporting Variants
Samples
Known GenesAK3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704836
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.870968


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