A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13697771



Internal ID21219627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90495859..90495960hg38UCSC Ensembl
chr13:91148113..91148214hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793161
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13697771
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.5


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