A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5945500



Internal ID22720979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11444043..11468828hg38UCSC Ensembl
chr16:11537899..11562684hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3824786
hg1924786
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17372012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5945500
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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