A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475655



Internal ID21133208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:84759467..84760064hg38UCSC Ensembl
chr14:85225811..85226408hg19UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38598
hg19598
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021696
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475655
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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