A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505139



Internal ID20878405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75779000..76162659hg38UCSC Ensembl
chr16:75812898..76196557hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38383660
hg19383660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032743
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505139
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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