A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001103



Internal ID21910446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111903222..111908454hg38UCSC Ensembl
chr6:112224425..112229657hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385233
hg195233
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17567863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001103
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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