A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008260



Internal ID21917603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:30987246..30987337hg38UCSC Ensembl
chr6:30955023..30955114hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572947
Samples
Known GenesMUC21
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008260
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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