A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6482884



Internal ID21140437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:24097704..24099071hg38UCSC Ensembl
chr14:24566913..24568280hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg381368
hg191368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016796
Samples
Known GenesPCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6482884
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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