A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752791



Internal ID20528651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73205675..73205675hg38UCSC Ensembl
chr6:73915398..73915398hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752791
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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