A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484947



Internal ID21142500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84299048..84299613hg38UCSC Ensembl
chr14:84765392..84765957hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022315
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484947
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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