A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13704566



Internal ID21226374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:23704137..23704137hg38UCSC Ensembl
chr9:23704135..23704135hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819574
Supporting Variants
Samples
Known GenesELAVL2
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13704566
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.166667


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