A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3953293



Internal ID21373363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56568221..56568270hg38UCSC Ensembl
chr16:56602133..56602182hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15176420
SamplesHG002
Known GenesMT4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3953293
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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