A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6492044



Internal ID21149597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24198126..24205489hg38UCSC Ensembl
chr14:24667332..24674695hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg387364
hg197364
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016798
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6492044
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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