A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15827216



Internal ID1917157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:27786920..27801779hg38UCSC Ensembl
chr18:25366884..25381743hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg3814860
hg1914860
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642049
Supporting Variants
SamplesHG01795
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15827216
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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