A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696963



Internal ID21218815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56703069..56703069hg38UCSC Ensembl
chr11:56470545..56470545hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811069
hg1911069
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2790429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696963
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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