A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012788



Internal ID21922131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:28089448..28089513hg38UCSC Ensembl
chr6:28057226..28057291hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570498
Samples
Known GenesZNF165
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012788
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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