A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006722



Internal ID21916065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:155218953..155219025hg38UCSC Ensembl
chr6:155540087..155540159hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566850
Samples
Known GenesTIAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006722
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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