A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641616



Internal ID6681701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4151476..4171783hg38UCSC Ensembl
chr18:4151476..4171783hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg3820308
hg1920308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15780366, essv15780364, essv15780363, essv15780365, essv15780362
SamplesNA19923, HG02953, HG03565, HG03258, HG03376
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641616
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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