A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476916



Internal ID21134469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78764987..78770148hg38UCSC Ensembl
chr14:79231330..79236491hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg385162
hg195162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020919
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476916
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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