A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6484719



Internal ID21142272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:78879949..78880261hg38UCSC Ensembl
chr14:79346292..79346604hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020926
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6484719
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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