A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500652



Internal ID20873880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24195101..24203900hg38UCSC Ensembl
chr16:24206422..24215221hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2735n223
Supporting Variantsnssv18182630
Samples
Known GenesPRKCB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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