A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13692942



Internal ID21214794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:91293320..91293553hg38UCSC Ensembl
chr14:91759664..91759897hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2794600
Supporting Variants
Samples
Known GenesCCDC88C
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13692942
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.517857


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