A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515280



Internal ID20888639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:48758477..48759754hg38UCSC Ensembl
chr16:48792388..48793665hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg381278
hg191278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029937
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515280
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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