A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13689481



Internal ID21211336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10129135..10129135hg38UCSC Ensembl
chr21:10607163..10607163hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2803456
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13689481
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.451613


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