A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515081



Internal ID20888438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:48111471..48115238hg38UCSC Ensembl
chr15:48403668..48407435hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg383768
hg193768
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024705
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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