A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17376802



Internal ID22602471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:60384297..60384484hg38UCSC Ensembl
chr16:60418201..60418388hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38188
hg19188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935153
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17376802
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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