A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514175



Internal ID20887527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23428201..25033300hg38UCSC Ensembl
chr15:23673348..25278447hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381605100
hg191605100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179964
Samples
Known GenesMAGEL2, MIR4508, MKRN3, NDN, NPAP1, PWAR5, PWARSN, PWRN1, PWRN2, SNORD107, SNORD108, SNORD64, SNRPN, SNURF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514175
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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