A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096952



Internal ID21489235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:29821715..29821715hg38UCSC Ensembl
chr16:29833036..29833036hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382090
hg192090
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655935
Supporting Variants
SamplesNA18939
Known GenesMVP, PAGR1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096952
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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