A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503192



Internal ID20876444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59007099..59012835hg38UCSC Ensembl
chr16:59041003..59046739hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg385737
hg195737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030902
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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