A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4752275



Internal ID20528135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:7673795..7673795hg38UCSC Ensembl
chr2:7813926..7813926hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294047
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4752275
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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