A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497304



Internal ID20870510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10810501..10824700hg38UCSC Ensembl
chr16:10904358..10918557hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3814200
hg1914200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18181977
Samples
Known GenesTVP23A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497304
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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