A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504787



Internal ID20878050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24120664..24450329hg38UCSC Ensembl
chr15:24365811..24695476hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38329666
hg19329666
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2397n223
Supporting Variantsnssv18023477
Samples
Known GenesPWRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504787
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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