A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513539



Internal ID20886884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69943630..70166599hg38UCSC Ensembl
chr16:69977533..70200502hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38222970
hg19222970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2915n223
Supporting Variantsnssv18031243
Samples
Known GenesCLEC18A, MIR1972-1, MIR1972-2, PDPR, PDXDC2P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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