A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514462



Internal ID20887815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19978401..19981400hg38UCSC Ensembl
chr16:19989723..19992722hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028178
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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