A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501014



Internal ID20874244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:47848451..47849309hg38UCSC Ensembl
chr15:48140648..48141506hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177414
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501014
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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