A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513877



Internal ID20887226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77095541..77119615hg38UCSC Ensembl
chr16:77129438..77153512hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3824075
hg1924075
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18194425
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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