A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088837



Internal ID21464715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56406277..56406277hg38UCSC Ensembl
chr16:56440189..56440189hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5657270
Supporting Variants
SamplesHG03065
Known GenesAMFR
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088837
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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