A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477083



Internal ID21134636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74783232..74787728hg38UCSC Ensembl
chr14:75249935..75254431hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384497
hg194497
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18021108
Samples
Known GenesYLPM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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