A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6501562



Internal ID20874797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72231333..72233906hg38UCSC Ensembl
chr15:72523674..72526247hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382574
hg192574
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026574
Samples
Known GenesPKM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6501562
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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