A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019689



Internal ID21929032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:42864053..42864228hg38UCSC Ensembl
chr6:42831791..42831966hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38176
hg19176
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564745
Samples
Known GenesGLTSCR1L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019689
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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