A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026783



Internal ID21936126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99602667..99602755hg38UCSC Ensembl
chr15:100142872..100142960hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17612222
Samples
Known GenesMEF2A
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026783
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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