A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506954



Internal ID20880242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:19732901..19792917hg38UCSC Ensembl
chr16:19744223..19804239hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3860017
hg1960017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18193319
Samples
Known GenesIQCK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506954
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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