A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13678998



Internal ID21200859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87863777..87863777hg38UCSC Ensembl
chr13:88516032..88516032hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2793153
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13678998
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.640625


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