A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510946



Internal ID20884269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21096478..21120303hg38UCSC Ensembl
chr16:21107799..21131624hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3823826
hg1923826
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185550
Samples
Known GenesDNAH3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510946
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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