A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513657



Internal ID20887003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56871922..56873587hg38UCSC Ensembl
chr16:56905834..56907499hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg381666
hg191666
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182353
Samples
Known GenesSLC12A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513657
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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