A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641895



Internal ID7028666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:14412454..14426967hg38UCSC Ensembl
Innerchr18:14412454..14426967hg38UCSC Ensembl
Outerchr18:14411954..14427467hg38UCSC Ensembl
chr18:14412453..14426966hg19UCSC Ensembl
Innerchr18:14412453..14426966hg19UCSC Ensembl
Outerchr18:14411953..14427466hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3814514
hg1914514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15815033, essv15815034, essv15815035
SamplesNA19315, NA18953, NA19331
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641895
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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