A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488687



Internal ID21146240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58302901..58307600hg38UCSC Ensembl
chr14:58769619..58774318hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019884
Samples
Known GenesARID4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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