A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510603



Internal ID20883923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42129212..42141617hg38UCSC Ensembl
chr15:42421410..42433815hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3812406
hg1912406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023928
Samples
Known GenesPLA2G4F
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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