A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087144



Internal ID21434096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51019963..51019963hg38UCSC Ensembl
chr16:51053874..51053874hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5649114
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087144
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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