A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514652



Internal ID20888007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89186252..89187071hg38UCSC Ensembl
chr16:89252660..89253479hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179777
Samples
Known GenesCDH15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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