A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685611



Internal ID21207471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:109569223..109569324hg38UCSC Ensembl
chr13:110221570..110221671hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38102
hg19102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2792159
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685611
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.482143


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