A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740114



Internal ID20516089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:131482064..131482175hg38UCSC Ensembl
chr6:131803204..131803315hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280310
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740114
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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