A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513125



Internal ID20886465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52702989..52749210hg38UCSC Ensembl
chr15:52995186..53041407hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3846222
hg1946222
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184418
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513125
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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