A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047406



Internal ID21956639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35143518..35143518hg38UCSC Ensembl
chr1:35609119..35609119hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536325
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047406
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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