A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511155



Internal ID20884481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:27683957..27721362hg38UCSC Ensembl
chr15:27929103..27966508hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3837406
hg1937406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18023746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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