A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472139



Internal ID22530031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57403424..57407387hg38UCSC Ensembl
chr16:57437336..57441299hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg383964
hg193964
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5871198
Supporting Variants
Samples
Known GenesCCL17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472139
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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