A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5657503



Internal ID21605808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:58119961..58119961hg38UCSC Ensembl
chr16:58153865..58153865hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38153
hg19153
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17094888
SamplesHG00171
Known GenesC16orf80
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5657503
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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