A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498276



Internal ID20871485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77743026..77745332hg38UCSC Ensembl
chr16:77776923..77779229hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg382307
hg192307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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