A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503282



Internal ID20876535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12401501..12423708hg38UCSC Ensembl
chr16:12495358..12517565hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3822208
hg1922208
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184752
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503282
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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