A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4751860



Internal ID20527720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:45643030..45643030hg38UCSC Ensembl
chr6:45610767..45610767hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16266064
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4751860
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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