A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011572



Internal ID21920915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:106670901..106681390hg38UCSC Ensembl
chr6:107118776..107129265hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3810490
hg1910490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562300
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011572
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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