A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5871198



Internal ID22646135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57403424..57407387hg38UCSC Ensembl
chr16:57437336..57441299hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383964
hg193964
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17472139
Samples
Known GenesCCL17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5871198
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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