A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500756



Internal ID20873984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:62182543..62204005hg38UCSC Ensembl
chr16:62216447..62237909hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3821463
hg1921463
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18197076
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500756
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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