A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4743968



Internal ID20519961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:54604921..54605032hg38UCSC Ensembl
chr6:54469719..54469830hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16282252
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4743968
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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