A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509217



Internal ID20882525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24187325..24576277hg38UCSC Ensembl
chr15:24432472..24821424hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38388953
hg19388953
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2406n223
Supporting Variantsnssv18189998
Samples
Known GenesPWRN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509217
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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