A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504064



Internal ID20877323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24786733..25084119hg38UCSC Ensembl
chr15:25031880..25329266hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38297387
hg19297387
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187491
Samples
Known GenesPWAR5, PWARSN, SNORD107, SNORD108, SNORD109A, SNORD109B, SNORD116-1, SNORD116-10, SNORD116-11, SNORD116-12, SNORD116-13, SNORD116-14, SNORD116-15, SNORD116-16, SNORD116-17, SNORD116-19, SNORD116-2, SNORD116-3, SNORD116-4, SNORD116-5, SNORD116-6, SNORD116-7, SNORD116-8, SNORD116-9, SNORD64, SNRPN, SNURF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504064
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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