A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491157



Internal ID21148710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:56892918..56893771hg38UCSC Ensembl
chr14:57359636..57360489hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38854
hg19854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18019793
Samples
Known GenesOTX2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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