A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4749923



Internal ID20525958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27270518..27270579hg38UCSC Ensembl
chr6:27238297..27238358hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16261383
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4749923
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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