A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178178



Internal ID20745218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8562878..8642685hg38UCSC Ensembl
chr16:8612880..8736542hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3879808
hg19123663
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503070
Supporting Variants
Samples
Known GenesMETTL22, TMEM114
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178178
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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