A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740625



Internal ID20516601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3618911..3621593hg38UCSC Ensembl
chr6:3619145..3621827hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382683
hg192683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740625
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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