A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487337



Internal ID21144890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:21624315..21624936hg38UCSC Ensembl
chr14:22092468..22093089hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg38622
hg19622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016039
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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