A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083485



Internal ID21453877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57628889..57628940hg38UCSC Ensembl
chr16:57662801..57662852hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5599767
Supporting Variants
SamplesHG02011
Known GenesGPR56
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083485
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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