A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513244



Internal ID20886586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3055722..3075599hg38UCSC Ensembl
chr16:3105723..3125600hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819878
hg1919878
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192948
Samples
Known GenesIL32, MMP25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513244
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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