A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14878543



Internal ID3137759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Cytoband
Allele length
AssemblyAllele length
hg38n/a
hg192294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633358
Supporting Variants
SamplesHG02768
Known GenesNALCN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14878543
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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