A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4748005



Internal ID20524028
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3310320..3310378hg38UCSC Ensembl
chr6:3310554..3310612hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16293371
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4748005
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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