A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512844



Internal ID20886183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79217882..79218520hg38UCSC Ensembl
chr15:79510224..79510862hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38639
hg19639
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196551
Samples
Known GenesLOC729911
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512844
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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