A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479571



Internal ID21137124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:58199801..58200400hg38UCSC Ensembl
chr14:58666519..58667118hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019877
Samples
Known GenesACTR10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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