A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487114



Internal ID21144667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79157901..79158700hg38UCSC Ensembl
chr14:79624244..79625043hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020947
Samples
Known GenesNRXN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487114
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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