A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17375935



Internal ID22601604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28338446..28339015hg38UCSC Ensembl
chr16:28349767..28350336hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5929298
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17375935
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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