A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514886



Internal ID20888241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87652238..87655616hg38UCSC Ensembl
chr16:87685844..87689222hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383379
hg193379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033648
Samples
Known GenesJPH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514886
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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