A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744905



Internal ID20520909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40244463..40244526hg38UCSC Ensembl
chr15:40536664..40536727hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16272222
Samples
Known GenesPAK6
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744905
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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