A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6478152



Internal ID21135705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20321047..20323846hg38UCSC Ensembl
chr14:20789206..20792005hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg382800
hg192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016544
Samples
Known GenesCCNB1IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6478152
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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