A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513284



Internal ID20886626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58910701..58920300hg38UCSC Ensembl
chr16:58944605..58954204hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2891n223
Supporting Variantsnssv18030889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513284
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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