A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514101



Internal ID20887452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45507901..45508273hg38UCSC Ensembl
chr15:45800099..45800471hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38373
hg19373
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024613
Samples
Known GenesSLC30A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514101
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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