A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5935576



Internal ID22710920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60131339..60131644hg38UCSC Ensembl
chr16:60165243..60165548hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17376525
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5935576
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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