A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499521



Internal ID20872742
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69299432..69300620hg38UCSC Ensembl
chr16:69333335..69334523hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg381189
hg191189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031780
Samples
Known GenesSNTB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499521
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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