A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509124



Internal ID20882430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10691133..10695425hg38UCSC Ensembl
chr16:10784990..10789282hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg384293
hg194293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180887
Samples
Known GenesTEKT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509124
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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