A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500168



Internal ID20873393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:64033269..64134304hg38UCSC Ensembl
chr16:64067173..64168208hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38101036
hg19101036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031017
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500168
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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