A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036418



Internal ID21945761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73562171..73562713hg38UCSC Ensembl
chr15:73854512..73855054hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38543
hg19543
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17609989
Samples
Known GenesNPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036418
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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