A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508763



Internal ID20882067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89665283..89665566hg38UCSC Ensembl
chr16:89731691..89731974hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033789
Samples
Known GenesSPATA33
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508763
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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