A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488510



Internal ID21146063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:47237201..47248600hg38UCSC Ensembl
chr14:47706404..47717803hg19UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2143n223
Supporting Variantsnssv18019284
Samples
Known GenesMDGA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488510
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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