A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689579



Internal ID21211433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68691333..68691625hg38UCSC Ensembl
chr15:68983672..68983964hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2795279
Supporting Variants
Samples
Known GenesCORO2B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689579
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.923077


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