A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017128



Internal ID21926471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:107975939..107976001hg38UCSC Ensembl
chr6:108297143..108297205hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562701
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017128
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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