A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372113



Internal ID22597782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11237946..11238850hg38UCSC Ensembl
chr16:11331803..11332707hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38905
hg19905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939255
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372113
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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