A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635044



Internal ID7021844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:79308556..79327914hg38UCSC Ensembl
chr14:79774899..79794257hg19UCSC Ensembl
Cytoband14q31.1
Allele length
AssemblyAllele length
hg3819359
hg1919359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15074345
SamplesNA18876
Known GenesNRXN3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635044
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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