A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643118



Internal ID6683198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74454714..74614537hg38UCSC Ensembl
chr18:72121949..72281773hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38159824
hg19159825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15934077, essv15934076
SamplesHG02394, NA20768
Known GenesCNDP1, CNDP2, FAM69C, LINC00909
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643118
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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