A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641770



Internal ID7028541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10286519..10292800hg38UCSC Ensembl
Innerchr18:10286519..10292800hg38UCSC Ensembl
Outerchr18:10286315..10292938hg38UCSC Ensembl
chr18:10286516..10292797hg19UCSC Ensembl
Innerchr18:10286516..10292797hg19UCSC Ensembl
Outerchr18:10286312..10292935hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg386282
hg196282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15804427, essv15804426, essv15804425
SamplesHG01083, HG02471, HG02716
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641770
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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