A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496019



Internal ID20869217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:73562063..73562794hg38UCSC Ensembl
chr15:73854404..73855135hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192115
Samples
Known GenesNPTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496019
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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