A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17371125



Internal ID22596794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30579926..30580225hg38UCSC Ensembl
chr16:30591247..30591546hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38300
hg19300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5945925
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17371125
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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