A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513570



Internal ID20886916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:59798601..59810400hg38UCSC Ensembl
chr16:59832505..59844304hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3811800
hg1911800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513570
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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