A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17374130



Internal ID22599799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10834320..10834371hg38UCSC Ensembl
chr16:10928177..10928228hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5934007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17374130
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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