A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496132



Internal ID20869330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89021303..89187011hg38UCSC Ensembl
chr16:89087711..89253419hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38165709
hg19165709
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18183665
Samples
Known GenesACSF3, CDH15, LINC00304, LOC400558
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496132
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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