A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504827



Internal ID20878090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55808701..55810100hg38UCSC Ensembl
chr16:55842613..55844012hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2888n223
Supporting Variantsnssv18185457
Samples
Known GenesCES1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504827
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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