A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5901454



Internal ID22676604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41073934..41075009hg38UCSC Ensembl
chr6:41041673..41042748hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381076
hg191076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17436606
Samples
Known GenesNFYA
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5901454
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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