A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497666



Internal ID20870874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88648761..88649082hg38UCSC Ensembl
chr16:88715169..88715490hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033217
Samples
Known GenesCYBA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497666
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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