A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497353



Internal ID20870559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79964143..80127537hg38UCSC Ensembl
chr15:80256485..80419879hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38163395
hg19163395
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182214
Samples
Known GenesBCL2A1, ZFAND6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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