A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376206



Internal ID22601875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51831363..51832238hg38UCSC Ensembl
chr16:51865274..51866149hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38876
hg19876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928635
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376206
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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