A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6054368



Internal ID21963601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7803433..7803433hg38UCSC Ensembl
chr1:7863493..7863493hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg38170
hg19170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17521463
Samples
Known GenesPER3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6054368
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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