A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641661



Internal ID7028435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5927626..5934107hg38UCSC Ensembl
Innerchr18:5927627..5934106hg38UCSC Ensembl
Outerchr18:5927625..5934108hg38UCSC Ensembl
chr18:5927625..5934106hg19UCSC Ensembl
Innerchr18:5927626..5934105hg19UCSC Ensembl
Outerchr18:5927624..5934107hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386482
hg196482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15792897, essv15792896, essv15792903, essv15792894, essv15792892, essv15792902, essv15792893, essv15792895, essv15792899, essv15792890, essv15792891, essv15792898, essv15792901, essv15792900
SamplesNA18502, NA18510, NA19446, HG02922, HG02111, NA19383, HG02009, HG03511, NA18933, NA19327, HG02283, NA19390, HG01205, HG02938
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641661
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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