A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704355



Internal ID21226160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:67538297..67538625hg38UCSC Ensembl
chr9:65906803..65907123hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38329
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704355
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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