A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707794



Internal ID21229584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121092468..121092543hg38UCSC Ensembl
chr9:123854746..123854821hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2819055
Supporting Variants
Samples
Known GenesCNTRL
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707794
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.765625


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