A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6034100



Internal ID21943443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3708903..3709025hg38UCSC Ensembl
chr16:3758904..3759026hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17599415
Samples
Known GenesTRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6034100
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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