A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934460



Internal ID22709787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11237990..11243703hg38UCSC Ensembl
chr16:11331847..11337560hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg385714
hg195714
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17383618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934460
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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