A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514268



Internal ID20887620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29784569..29786981hg38UCSC Ensembl
chr16:29795890..29798302hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382413
hg192413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029118
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514268
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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