A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054382



Internal ID21963615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:114907011..114907011hg38UCSC Ensembl
chr1:115449632..115449632hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530357
Samples
Known GenesSYCP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054382
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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