A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504774



Internal ID20878037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63831156..63919744hg38UCSC Ensembl
chr16:63865060..63953648hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3888589
hg1988589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030996
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504774
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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