A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4753541



Internal ID20529401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:130613181..130613181hg38UCSC Ensembl
chr6:130934326..130934326hg19UCSC Ensembl
Cytoband6q23.1
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16276288
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4753541
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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