A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5942616



Internal ID22718056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56704076..56704437hg38UCSC Ensembl
chr16:56737988..56738349hg19UCSC Ensembl
Cytoband16q13
Allele length
AssemblyAllele length
hg38362
hg19362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17378935
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5942616
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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