A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012476



Internal ID21921819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:23034514..23053346hg38UCSC Ensembl
chr6:23034743..23053574hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3818833
hg1918832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012476
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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