A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4742191



Internal ID20518171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41087381..41088239hg38UCSC Ensembl
chr6:41055120..41055978hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285261
Samples
Known GenesNFYA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4742191
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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