A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643283



Internal ID6683363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:79003881..79112789hg38UCSC Ensembl
chr18:76763881..76872789hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38108909
hg19108909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15955824
SamplesNA06984
Known GenesATP9B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643283
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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