A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498118



Internal ID20871326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:72378919..72576831hg38UCSC Ensembl
chr16:72412818..72610730hg19UCSC Ensembl
Cytoband16q22.2
Allele length
AssemblyAllele length
hg38197913
hg19197913
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178049
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498118
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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