A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507863



Internal ID20881159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11338312..11450114hg38UCSC Ensembl
chr16:11432169..11543970hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38111803
hg19111802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187177
Samples
Known GenesRMI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507863
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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