A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17372134



Internal ID22597803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9394066..9394396hg38UCSC Ensembl
chr16:9487923..9488253hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5927608
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17372134
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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