A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051016



Internal ID21960250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28332716..28332716hg38UCSC Ensembl
chr1:28659227..28659227hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17517783
Samples
Known GenesMED18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051016
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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