A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009870



Internal ID21919213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:39284874..39284943hg38UCSC Ensembl
chr6:39252650..39252719hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576824
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009870
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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