A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767073



Internal ID20542933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:45579434..45579434hg38UCSC Ensembl
chr10:46074882..46074882hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38295
hg19295
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282711
Samples
Known GenesMARCH8
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767073
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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