A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4759931



Internal ID20535791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3776795..3776795hg38UCSC Ensembl
chr6:3777029..3777029hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38681
hg19681
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16294122
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4759931
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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