A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747397



Internal ID20523416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42753920..42753978hg38UCSC Ensembl
chr6:42721658..42721716hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264451
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747397
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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