A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6026908



Internal ID21936251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:76259376..76259433hg38UCSC Ensembl
chr15:76551717..76551774hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600760
Samples
Known GenesETFA, TYRO3P
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6026908
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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