A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014087



Internal ID21923430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3978410..3978476hg38UCSC Ensembl
chr6:3978644..3978710hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561176
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014087
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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