A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6085283



Internal ID21994516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:51137966..51137966hg38UCSC Ensembl
chr16:51171877..51171877hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17626436
Samples
Known GenesSALL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6085283
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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