A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643203



Internal ID7029972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77102167..77103293hg38UCSC Ensembl
Innerchr18:77102217..77103243hg38UCSC Ensembl
Outerchr18:77102117..77103343hg38UCSC Ensembl
chr18:74814123..74815249hg19UCSC Ensembl
Innerchr18:74814173..74815199hg19UCSC Ensembl
Outerchr18:74814073..74815299hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381127
hg191127
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15944397, essv15944398
SamplesHG03995, HG03896
Known GenesMBP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643203
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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