A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498672



Internal ID20871885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23283208..23284202hg38UCSC Ensembl
chr16:23294529..23295523hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg38995
hg19995
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498672
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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