A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503722



Internal ID20876978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101486791..101773813hg38UCSC Ensembl
chr15:102026996..102314016hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38287023
hg19287021
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191602
Samples
Known GenesPCSK6, TARSL2, TM2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503722
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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