A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477294



Internal ID21134847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:83706180..83706587hg38UCSC Ensembl
chr14:84172524..84172931hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38408
hg19408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477294
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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