A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508803



Internal ID20882107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69971816..70194596hg38UCSC Ensembl
chr16:70005719..70228499hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38222781
hg19222781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2915n223
Supporting Variantsnssv18031244
Samples
Known GenesCLEC18C, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508803
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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