A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484187



Internal ID21141740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84172949..84173508hg38UCSC Ensembl
chr14:84639293..84639852hg19UCSC Ensembl
Cytoband14q31.2
Allele length
AssemblyAllele length
hg38560
hg19560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18022299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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