A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042876



Internal ID21952188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5691880..5693405hg38UCSC Ensembl
chr7_gl000195_random:4610..6135hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg381526
hg191526
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042876
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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