A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478486



Internal ID21136039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61307282..61312342hg38UCSC Ensembl
chr14:61774000..61779060hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg385061
hg195061
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478486
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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