A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053756



Internal ID21962989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52931862..52931862hg38UCSC Ensembl
chr1:53397534..53397534hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17537462
Samples
Known GenesSCP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053756
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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