A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642307



Internal ID7029077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:40779205..40819673hg38UCSC Ensembl
Innerchr18:40779234..40819645hg38UCSC Ensembl
Outerchr18:40779177..40819702hg38UCSC Ensembl
chr18:38359169..38399637hg19UCSC Ensembl
Innerchr18:38359198..38399609hg19UCSC Ensembl
Outerchr18:38359141..38399666hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg3840469
hg1940469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15851313
SamplesHG02127
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642307
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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