A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977199



Internal ID22752134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53950155..53950155hg38UCSC Ensembl
chr16:53984067..53984067hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17389218
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977199
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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