A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6024008



Internal ID21933351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73572543..73572621hg38UCSC Ensembl
chr15:73864884..73864962hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17613533
Samples
Known GenesNPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6024008
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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