A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6483396



Internal ID21140949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:22612378..22614974hg38UCSC Ensembl
chr14:23081284..23083877hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382597
hg192594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016078
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6483396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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