A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480537



Internal ID21138090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63596512..63602980hg38UCSC Ensembl
chr14:64063230..64069698hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg386469
hg196469
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020637
Samples
Known GenesWDR89
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480537
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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