A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5943620



Internal ID22719071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3709857..3711083hg38UCSC Ensembl
chr16:3759858..3761084hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17377266
Samples
Known GenesTRAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5943620
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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